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WormGuy

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  1. Thanks for the prayers,they are welcomed. And now for more news... I went to my urologist yesterday & he informed me I have blood in my urine. He said he could be a stone that is up high, a bladder tumor, or the cancer is back. I go the first of December for ultrasound and test. I'm wondering if this is what is causing my back pain. John
  2. http://www.fda.gov/Safety/Recalls/ucm528271.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. SHRI SHIVA Foods Inc. Recalls "MTR Sambar Powder" Because Of Possible Health Risk For Immediate Release November 7, 2016 Contact Consumers Consumer Affairs 347-581-7931 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm528271.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Long Island City, NY - SHRI SHIVA Foods Inc. is recalling MTR Sambar Powder, Net Quantity: 200 g (LOT NO# 15J27C, MFD.27.10.15) because it may be contaminated with Salmonella, with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea,vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. The product was sold between January 2016 to October 2016 thru one NY and one OH via wholesaler. Product is packed in 200g plastic pouches under MTR Brand stamped with MFD.27.10.15 on the back. No illnesses have been reported to date. The U.S. Food and Drug Administration discovered the potential contamination through previous product sampling. Consumers who have purchased the product are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company's consumer affairs at 347-581-7931, Monday through Friday 10am-5pm, EST. John
  3. http://www.fda.gov/Safety/Recalls/ucm528284.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Ton Shen Health Recalls Life Rising Brand “Side Head Regulator TT Tablet” Because of Possible Health Risk for Children Under the Age of 18 For Immediate Release November 7, 2016 Contact Consumers 1-312-842-2775 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm528284.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Ton Shen Health of Chicago, IL, is recalling its Life Rising brand “Side Head Regulator TT” Tablets because they have tested positive for elevated levels of lead for children under the age of 18. Lead is a naturally occurring element which can affect multiple body systems and is particularly harmful to young children. Recent lab tests indicate certain lots of TT product have elevated levels of lead above the currently recognized acceptable levels for children. Lead poisoning can happen if a person is exposed to high levels of lead over short periods of time. Due to the test results affecting children and to the possibility of use by children, Ton Shen Health is recalling the TT product. The recalled Life Rising brand "Side Head Regulator TT" tablets were mostly sold locally in Chicago area retail stores and some were distributed to other states through mail orders. The product comes in a 1.6 ounce, white plastic package marked with lot # on the bottom. UPC: 616042101010 People with high blood levels of lead may show no symptoms, but the condition may cause damage to the nervous system and internal organs. Acute lead poisoning may cause a wide range of symptoms, including abdominal pain, muscle weakness, nausea, vomiting, diarrhea, weight loss, and bloody or decreased urinary output. Children are particularly vulnerable to lead poisoning. Lead poisoning can be diagnosed through clinical testing, and individuals who have consumed TT Side Head Regulator should talk to their health care providers about testing. If a child is exposed to enough lead for a protracted period of time (e.g., weeks to months) permanent damage to the central nervous system can occur. This can result in learning disorders, developmental defects, and other long-term health problems. The extent of the functional detriment is dependent on the duration and degree of exposure. Such an outcome may occur if this product containing the reported level of lead were consumed by children in such a way. No illnesses have been reported to date in connection with this product, but the tablets have been tested and due to the elevated level of lead for children presently in TT samples tested, all TT products distributed by Ton Shen Health are being recalled. The elevated lead level for children was noted after FDA tested a sample of TT tablets that were provided to the FDA. This recall is precautionary in nature, but important for all users of this product to comply with and make sure any TT products in their possession are not consumed by children and returned for a refund or destroyed. The sale of the product has been suspended by Ton Shen Health effective end of September of 2016. Consumers who have purchased Side Head Regulator TT tablets are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-312-842-2775 central standard time, Monday to Friday, from 9:30AM to 5:00PM. John
  4. http://www.fda.gov/Drugs/ResourcesForYou/Consumers/BuyingUsingMedicineSafely/MedicationHealthFraud/ucm528280.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Public Notification: Ultimate Body Tox contains hidden drug ingredient 11-7-2016 The Food and Drug Administration (FDA) is advising consumers not to purchase or use Ultimate Body Tox, a product promoted and sold for weight loss on various Web sites, including www.ultimatebodytox.com, and possibly in some retail stores. FDA laboratory analysis confirmed that Ultimate Body Tox contains sibutramine. Sibutramine is a controlled substance that was removed from the market in October 2010 for safety reasons. The product poses a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. This product may also interact, in life-threatening ways, with other medications a consumer may be taking. Health care professionals and patients are encouraged to report adverse events or side effects related to the use of this product to FDA's MedWatch Safety Information and Adverse Event Reporting Program: Complete and submit the report online MedWatch Online Voluntary Reporting Form, https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=reporting.home or: Download and complete the form, http://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM349464.pdf then submit it via fax at 1-800-FDA-0178. Note: This notification is to inform the public of a growing trend of dietary supplements or conventional foods with hidden drugs and chemicals. These products are typically promoted for sexual enhancement, weight loss, and body building and are often represented as being “all natural.” FDA is unable to test and identify all products marketed as dietary supplements that have potentially harmful hidden ingredients. Consumers should exercise caution before purchasing any product in the above categories. Contact FDA Toll Free (855) 543-3784, or (301) 796-3400 druginfo@fda.hhs.gov Human Drug Information Division of Drug Information (CDER) Office of Communications Feedback Form 10001 New Hampshire Avenue Hillandale Building, 4th Floor Silver Spring, MD 20993 John
  5. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-103-2016-release News Release OSI Industries, LLC Recalls Chicken Products Due To Possible Foreign Matter Contamination Class II Recall 103-2016 Health Risk: Low Nov 6, 2016 Congressional and Public Affairs Allie Ryan (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Nov. 6, 2016 – OSI Industries, LLC, a Fort Atkinson, Wis. establishment, is recalling approximately 21,403 pounds of chicken products that may be contaminated with extraneous materials, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The ready-to-eat chicken products were produced on Aug. 5, 2016. The following products are subject to recall: View Labels PDF Only http://www.fsis.usda.gov/wps/wcm/connect/2c8d44f7-6609-4566-98f7-8ac7957cb787/103-2016-labels.pdf?MOD=AJPERES 35-oz./2 lbs 3 oz frozen plastic packages containing “ON-COR CHICKEN PATTIES MICROWAVEABLE” with Best by Date 8/5/2017 The products subject to recall bear establishment number “P-5615” inside the USDA mark of inspection. These items were shipped to retail locations in Kansas, Kentucky, Minnesota, North Carolina, Ohio and Wisconsin. The problem was discovered when the firm received notification of three consumer complaints mentioning firm blue plastic in their product. The product was contaminated around the time a trim repair was made on belt material. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. Consumers with questions about the recall can contact Dave Wetherton, Assistant VP of Retail Sales, at (844) 674-8100. Members of the media with questions about the recall can contact David Saltz, Media Coordinator, at (312) 203-2114. John
  6. http://www.fda.gov/Safety/Recalls/ucm528146.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Crescent Vending Co. Issues Allergy Alert on Undeclared (Wheat, Soy, Milk, And Egg) in Product For Immediate Release November 5, 2016 Contact Consumers 215-887-2213 Announcement Crescent Vending Company of Oreland, PA is recalling because they may contain an undeclared specific type of allergen. Product Allergens Good Thru Dates Bagel and Cream Cheese Wheat, Soy, Milk 10/28/2016 thru 11/10/2016 Raisin Bagel and Cream Cheese Wheat, Soy, Milk 10/28/2016 thru 11/10/2016 Egg Salad on Wheat Bread Wheat, Soy, Egg 11/4/2016 thru 11/6/2016 Cheeseburger Wheat, Soy, Milk 11/1/2016 thru 11/7/2016 Hot Sausage on Club Roll Wheat, Soy 11/2/2016 thru 11/7/2016 Turkey Bacon and Swiss on Kaiser with Macaroni Salad Wheat, Soy, Milk, Egg 11/4/2016 thru 11/6/2016 3oz. Imported Ham with Potato Salad Wheat, Soy, Milk, Egg 11/4/2016 thru 11/6/2016 Roast Beef and Cheddar on Kaiser Wheat, Soy, Milk 11/4/2016 thru 11/6/2016 Ham and Cheese on Club Roll Wheat, Soy, Milk 11/4/2016 thru 11/7/2016 Chicken Salad on Kaiser Wheat, Soy 11/3/2016 thru 11/5/2016 Turkey Club Wheat, Soy 11/3/2016 thru 11/4/2016 Regular Hoagie on Italian Roll Wheat, Soy, Milk 11/3/2016 thru 11/4/2016 Meatball with Cole Slaw Wheat, Soy, Milk, Egg 11/3/2016 thru 11/6/2016 Bacon Egg and Cheese on Kaiser Wheat, Soy, Milk, Egg 11/2/2016 thru 11/5/2016 Turkey Bacon and Swiss on Kaiser Wheat, Soy, Milk 11/2/2016 thru 11/4/2016 Vegetable Dip Soy, Milk 11/2/2016 thru 11/5/2016 Mild Italian Sausage on Italian Roll Wheat, Soy 11/2/2016 thru 11/5/2016 Hot Sicilian-Ham Pepperoni and Provolone on Kaiser Wheat, Soy, Milk 11/2/2016 thru 11/5/2016 Sausage Egg and Cheese on Kaiser Wheat, Soy, Milk 11/2/2016 thru 11/5/2016 ¼ Lb. Hot Dog with Cheese on Italian Roll Wheat, Soy, Milk 11/1/2016 thru 11/4/2016 Salisbury Steak With Gravy and Whipped potatoes Wheat, Soy, Milk 11/1/2016 thru 11/4/2016 People who have an allergy or severe sensitivity to a specific type of allergen run the risk of serious or life-threatening allergic reaction if they consume products that have these allergens in them. The product was distributed in Montgomery County Pennsylvania where the product was distributed through the companies’ owned and operated refrigerated vending machines. The product has a Crescent Vending label on it and is wrapped in plastic film. The product has a weights between 4 oz. and 8 oz. and has a “Good thru” dates of 11/4/16 thru 11/10/16. No illnesses have been reported to date. The recall was initiated because the company did not have ingredient labels on the product. The allergens were not listed either. Consumers who have purchased product are urged to return it to Crescent Vending Co. for a full refund. Consumers with questions can contact the company at 215-887-2213 between the hours of 8:00am to 4:00pm Eastern Standard Time Monday to Friday. John
  7. http://www.fda.gov/Safety/Recalls/ucm528105.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. OLMA-XXI, Inc. Recalls Two Smoked Fish Products Because of Possible Health Risk For Immediate Release November 4, 2016 Contact Consumers OLMA-XXI, Inc. 718-675-0706 Media Igor Eliachov 718-675-0706 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm528105.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos OLMA-XXI, Inc. of Brooklyn, NY is recalling Premium Norwegian Salmon Smoked, Sliced 8 oz (227g), Best by 02/23/2017 and Salmon, Turbot, Butterfish, Smoked, Sliced 8 oz (227g), Best by 10/20/2016, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women. Premium Norwegian Salmon Smoked, Sliced 8 oz (227g), UPC #856687004288, lot #606002 - best by 02/23/2017 Salmon, Turbot, Butterfish Smoked, Sliced 8 oz (227g), UPC #856687004448, lot #529910- best by 10/20/2016 The items were distributed by refrigerated trucks through retail stores and warehouses between December 2015 to October 2016 in NY, NJ, MD, PA, MA, CA VA, FL, CT, TX, IL, GA & WA. Both items are packaged in a plastic vacuum packed bag. No illnesses have been reported to date. The recall was the result of a routine sampling program by the Florida Department of Agriculture and Consumer Services, Division of Food Safety which revealed the presence of Listeria monocytogenes. Consumers who have purchased the products are urged to return them to OLMA-XXI, Inc. for a full refund. Consumers with questions may contact the company at 718-675-0706, Monday – Friday, 8am – 6pm, ET. John
  8. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-101-2016-release News Release Gaiser's European Style Provision Inc. Recalls Chicken and Pork Bologna Products Due to Misbranding, Undeclared Allergens, and Being Formulated with Uninspected Meat and Poultry Products Class I Recall 101-2016 Health Risk: High Oct 26, 2016 Distribution List PDF http://www.fsis.usda.gov/wps/wcm/connect/aefef0de-c9d1-49d1-8d76-7c8fa51784ea/RC-101-2016-Retail-List.pdf?MOD=AJPERES&CONVERT_TO=url&CACHEID=aefef0de-c9d1-49d1-8d76-7c8fa51784ea Congressional and Public Affairs Maria Machuca (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Oct. 26, 2016 – Gaiser’s European Style Provision Inc., a Union, N.J. establishment, is recalling approximately 3,895 pounds of chicken and pork bologna products due to misbranding, undeclared allergens, and being formulated with meat and poultry products that were not federally inspected, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products may contain nonfat dry milk, a known allergen which is not declared on the finished product label. The bologna items were produced on various dates from Oct. 6, 2016 to Oct. 20, 2016. The following products are subject to recall: View Labels PDF only http://www.fsis.usda.gov/wps/wcm/connect/cf16a4d0-6bb3-48a5-ad5c-b6267d6fef29/101-2016-labels.pdf?MOD=AJPERES 1-lb. chubb artificial casing containing “Gaiser’s RUSSIAN BRAND PROFESSORSKAYA BOLOGNA” pork bologna with various packaging dates from Oct. 10, 2016 to Oct. 21, 2016. 10-lb. chubb artificial casing containing “Gaiser’s PROFESSORSKAYA” pork bologna with various packaging dates from Oct. 10, 2016 to Oct. 21, 2016. 1-lb. chubb artificial casing containing “NetCost Market PROFESSORSKAYA BRAND BOLOGNA” with various packaging dates from Oct. 10, 2016 to Oct. 21, 2016. 1-lb. chubb artificial casing containing “Gaiser’s CHICKEN BOLOGNA” with various packaging dates from Oct. 10, 2016 to Oct. 21, 2016. 3-lb. chubb artificial casing containing “Gaiser’s CHICKEN BOLOGNA” with various packaging dates from Oct. 10, 2016 to Oct. 21, 2016. 1-lb. chubb artificial casing containing “NetCost Market CHICKEN BOLOGNA” with various packaging dates from Oct. 10, 2016 to Oct. 21, 2016. The products subject to recall bear establishment number “EST. 5385 or P-5385” inside the USDA mark of inspection. These items were shipped to retail locations and/or for institutional use in California, Minnesota, New Jersey, New York and Washington. The problem was discovered during a Food Safety Assessment conducted by FSIS personnel. There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls. Consumers and members of the media with questions about the recall can contact Igor Denisenko, Gaiser’s European Style Provision Inc.’s plant manager, at (908) 686-3421. John
  9. http://www.fda.gov/Safety/Recalls/ucm528091.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. McConnell’s Fine Ice Creams Recalls Select 16oz. Packages Due To Possible Health Risk For Immediate Release November 4, 2016 Contact Consumers McConnell's Recall Hotline recall@mcconnells.com. 866-723-2454 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm528091.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos Santa Barbara, CA - Out of an abundance of caution, McConnell’s Fine Ice Creams is undertaking a voluntary recall of selected, 16 oz. (pint size) packages of ice cream produced by a contract manufacturer because they have the potential to be contaminated with Listeria monocytogenes. The seven affected flavors, available only in pints, accounts for approximately 15% of the pint-packaged ice cream products carrying the McConnell’s brand label. All of the recalled products were manufactured and packaged in a facility owned by a contract manufacturer, Dr. Bob’s of Upland, LLC. No other products were affected. Ice cream produced at McConnell’s Santa Barbara facility are not included in the recall. No illnesses have been reported. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infections can cause miscarriages and stillbirths among pregnant women. The U.S. Food and Drug Administration (FDA) found samples positive for Listeria monocytogenes in the contract manufacturer’s facility and in finished product of another company’s brand, leading the contract manufacturer to recall all ice cream products it produced for McConnell’s and other ice cream companies this year. Because this recall affects only McConnell’s products manufactured by the contract manufacturer facility, it is important that consumers carefully check the following flavor/code date combinations to be certain the correct products are removed. The following flavors and “Best By” code dates are being recalled: Dutchman’s Chocolate JUL 27 2017, OCT 01 2017 and OCT 05 2017 Mint Chip SEP 08 2017, SEP 30 2017, OCT 07 2017, DEC 01, 2017, DEC 30, 2017, JAN 04, 2018, JAN 05, 2018 Peppermint Stick JUL 25, 2017, JUL 26, 2017, SEP 30, 2017 Salted Caramel Chip OCT 07, 2017, OCT 20, 2017, DEC 22, 2017, JAN 06, 2018, JAN 07, 2018 Sweet Cream JUL 27, 2017, SEP 08, 2017, OCT 01, 2017, OCT 21, 2017, DEC 08, 2017, DEC 21, 2017, DEC 24, 2017 Turkish Coffee JUL 28, 2017, SEP 22, 2017, OCT 07, 2017, Dec 06, 2017 Vanilla Bean JUL 13, 2017, JUL 25, 2017, JUL 27, 2017, OCT 01, 2017, OCT 15, 2017, DEC 07, 2017, DEC 25, 2017, JAN 03, 2018, JAN 06, 2018 The recalled ice cream was distributed in AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, IA, KS, KY, LA, MA, MD, MI, MN, MS, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA and WI to retail stores. The product comes in a 16-ounce (pint size) paper package marked with “Best By” lot numbers listed above and printed in black on the bottom of the carton. Consumers who have purchased any of the seven 16-ounce (pint size) packages of McConnell’s ice cream should not eat these products and are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company recall hotline at 866-723-2454 between the hours of 8 am and 8 pm E.S.T., Monday through Friday. Customers may also contact McConnell’s by email at recall@mcconnells.com. John
  10. As some of you know I have have back problems for years. I have learned to live with the pain until now. For 43 years I have had back pain mainly on my left side. Now I have pain on my right side. I've been through traction, therapy, surgery, etc. I've worked, played (within limits), and lived the best I could. This new twist has really gotten me down. Some days it's all I can do to function. It's a new place for me to have pain and I don't like it. My doctor recommended aqua therapy and it was okay but I saw no benefits. The pain got too great and I had to stop. I went and had an MRI last week and I'm waiting to go see an neurosurgeon for an evaluation when they call me. I have no doubt they are going to want to do surgery and I'm just not comfortable with that at this time. I can still walk and drive which was something I could not do before I had surgery back in 1987. The point of this post is to let everyone know that there are days when I don't post anything due to what is going on. This means I have to play catch up and I don't like that. Bear with me if you can. I'll keep going until I get to the point it's too painful to sit and type as which point I will let you know. John
  11. http://www.fda.gov/Safety/Recalls/ucm528016.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Select Whole Foods Market Stores in Mid-Atlantic Region Issues Allergy Alert Due to Undeclared Eggs For Immediate Release November 3, 2016 Contact Consumers 301-984-4874 Announcement Rockville, Md. – Select Whole Foods Market stores in Pennsylvania, Maryland, Ohio, Kentucky, New Jersey, Virginia and Washington D.C. are voluntarily recalling batches of its Chocolate Croissants because the product contains eggs and the ingredient was not declared on product packaging. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product. This recall only applies to Whole Foods Market’s stores in its Mid-Atlantic region, which include 51 stores located throughout Pennsylvania, Maryland, Ohio, Kentucky, New Jersey, Virginia and Washington D.C. The recalled products were made and packaged in-house in clear plastic containers in counts of six. Each product also had a white label on top of the package that included the product name “Chocolate Croissants 6pk,” UPC0248422008994 and sell-by dates on or before Nov. 5, 2016. All affected product has already been removed from store shelves and no adverse reactions have been reported, to date. Customers who have purchased this product can bring the item or receipt into the store for a full refund. Customers with additional questions can contact Mid-Atlantic Regional Support Office: 301-984-4874. Please check the Whole Foods Market website to find the location and hours of the store nearest to you. John
  12. https://cpsc.gov/Recalls/2017/KTM-North-America-Recalls-Closed-Course-Competition-Off-Road-Motorcycles KTM North America Recalls Closed-Course/Competition Off-Road Motorcycles Due to Crash Hazard Recall date: November 3, 2016 Recall number: 17-027 Recall Summary Name of product: Closed-course/competition off-road motorcycles Hazard: The front brake master cylinder can malfunction, posing a crash hazard. Remedy: Repair Consumer Contact: KTM North America/Husqvarna Motorcycles North America toll-free at 888-985-6090 from 8 a.m. to 5 p.m. ET Monday through Friday or online at http://www.ktm.com/us/service/safety/ or www.husqvarna-motorcycles.com for more information. Recall Details Units: About 1,200 Description: This recall involves model year 2017 KTM brand and Husqvarna motorcycles brand closed-course/competition only motorcycles. Five KTM models are being recalled: 150 XC-W, 250 XC-W, 300 XC-W, 350 SX-F and 450 XC-F. Three Husqvarna models are being recalled: TC 250, TX 300 and FC 350. Recalled KTM motorcycles are orange and black with the KTM logo and engine size on both sides of the shrouds covering the fuel tank. Recalled Husqvarna motorcycles are white with blue and yellow markings and the Husqvarna logo on both sides of the shrouds covering the fuel tank. The engine size is located on both sides of the rear fender below the rear of the seat. Model year 2017 motorcycles have a letter “H” in the 10th position of the vehicle identification number (VIN), located on the right side of the steering head. Incidents/Injuries: None reported Remedy: Consumers should immediately stop using the recalled motorcycles and contact an authorized KTM or Husqvarna Motorcycles dealer to schedule a free repair. Sold At: KTM and Husqvarna Motorcycles authorized dealers nationwide from June 2016 to August 2016 for between $8,000 and $11,000. Importer(s): KTM North America, Inc., of Amherst, Ohio Distributor(s): KTM North America, Inc., of Amherst, Ohio Manufactured In: Austria John
  13. https://cpsc.gov/Recalls/2017/Trek-Recalls-Farley-Bicycles Trek Recalls Farley Bicycles Due to Fall Hazard Recall date: November 2, 2016 Recall number: 17-025 Recall Summary Name of product: Trek Farley bicycles and framesets Hazard: The fork can separate from the steer tube, posing a fall hazard to the rider. Remedy: Repair Consumer Contact: Trek at 800-373-4594 from 8 a.m. to 6 p.m. CT Monday through Friday or online at www.trekbikes.com and click on Safety & Recalls at the bottom of the page for more information. Recall Details In Conjunction With: Canadian Flag Units: About 2,600 (in addition, about 360 units were sold in Canada) Description: This recall involves model year 2014 Trek Farley bicycles and framesets and 2015 Trek Farley 6 bicycles and framesets. The 2014 Trek Farley is black with green decals with an aluminum frame and fork. The 2014 frameset is sky blue with orange decals. The 2015 Trek Farley 6 is black with blue decals with an aluminum frame and fork. Both bicycle models were sold in 14.5 through 21.5 inch sizes. “Trek” is printed across the bicycle frame. Incidents/Injuries: The firm has received five reports of the bicycle fork separating from the steer tube. No injuries have been reported. Remedy: Consumers should immediately stop using the recalled bicycles and framesets and return the bicycles to a Trek retailer for a free inspection and repair. Sold At: Bicycle stores nationwide from September 2013 through August 2016 for between $1,700 and $2,600. Importer(s): Trek Bicycle Corp., of Waterloo, Wis. Manufactured In: Taiwan John
  14. https://cpsc.gov/Recalls/2017/Dehumidifiers-Made-by-Midea-Recalled Dehumidifiers Made by Midea Recalled Due to Serious Fire and Burn Hazards; $4.8 Million in Property Damage Reported Recall date: November 2, 2016 Recall number: 17-024 Recall Summary Name of product: Dehumidifiers Hazard: The dehumidifiers can overheat, smoke and catch fire, posing serious fire and burn hazards. Remedy: Refund Replace Consumer Contact: GD Midea at 800-600-3055 from 7 a.m. to 6 p.m. CT Monday through Friday or online at www.midea.com/us/ and click on Product Recall for more information. Recall Details In Conjunction With: Canadian Flag Units: About 3.4 million (in addition 850,000 were sold in Canada) Description: This recall involves 25, 30, 40, 50, 60, 65, 70, and 75-pint dehumidifiers with the following brand names: Airworks, Alen, Arcticaire, Arctic King, Beaumark, Coolworks, ComfortAire, Comfort Star, Continental Electic, Crosley, Daewoo, Danby, Danby & Designer, Dayton, Degree, Diplomat, Edgestar, Excell, Fellini, Forest Air, Frigidaire, GE, Grunaire, Hanover, Honeywell, Homestyles, Hyundai, Ideal Air, Kenmore (Canada), Keystone, Kul, Midea, Nantucket, Ocean Breeze, Pelonis, Perfect Aire, Perfect Home, Polar Wind, Premiere, Professional Series, Royal Sovereign, Simplicity, Sunbeam, SPT, Sylvania, TGM, Touch Point, Trutemp, Uberhaus, Westpointe, Winix, and Winixl The brand name, model number, pint capacity and manufacture date are printed on the nameplate sticker on the back of the dehumidifier. To determine if your dehumidifier has been recalled, enter the model number at https://www.recallrtr.com/dehumidifier Incidents/Injuries: Midea has received 38 reports of smoke and fire. About $4.8 million property damage has been reported. No injuries have been reported. Remedy: Consumers should immediately turn off and unplug the dehumidifiers and contact GD Midea for either a replacement unit or a partial refund. Consumers whose dehumidifiers were manufactured before October 1, 2008 will receive a partial refund, not a replacement. The manufacturing dates can be found on back of units. Sold At: Lowes, Menards, PC Richard and other stores nationwide from January 2003 through December 2013 for between $100 and $300. Manufacturer(s): GD Midea Air Conditioning Equipment Ltd., of China Manufactured In: China John
  15. https://cpsc.gov/Recalls/2017/Pier-1-Imports-Recalls-Glass-Knobs Pier 1 Imports Recalls Glass Knobs Due to Laceration Hazard Recall date: November 2, 2016 Recall number: 17-026 Recall Summary Name of product: Glass knobs Hazard: The glass knobs can break while in use, posing a risk of laceration to users from broken glass pieces. Remedy: Refund Consumer Contact: Pier 1 Imports toll-free at 855-513-5140 from 8 a.m. to 7 p.m. CT Monday through Friday, 9 a.m. to 5 p.m. CT Saturday or 10 a.m. to 6 p.m. CT Sunday, or online at www.pier1.com and click on “Product Notes & Recalls” at the bottom of the page for more information. Recall Details In Conjunction With: Canadian Flag Units: About 140,000 units in the U.S. (in addition, about 17,600 units sold in Canada) Description: This recall involves Pier 1 Imports Basic, Kira and Facets glass knobs commonly used with dressers, cabinets and small drawers. The glass knobs have a metal stem affixed to one side and were sold in seven colors: clear, teal, pink, green, aquamarine, champagne and silver. No other decorative knobs are included in this recall. Incidents/Injuries: Pier 1 Imports has received seven reports of injuries as a result of glass knobs breaking during installation or while in use. Remedy: Consumers should immediately stop using the recalled glass knobs and return them to any Pier 1 Imports store for a full refund or merchandise credit. Sold Exclusively At: Pier 1 Imports stores nationwide and online at www.pier1.com from September 2011 through October 2016 for between $6 and $7. Importer(s): Pier 1 Imports, of Fort Worth, Texas Manufactured In: India John
  16. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-102-2016-release News Release Flavor Trade, LLC. Recalls Beef Products Produced Without Benefit of Inspection Class I Recall 102-2016 Health Risk: High Nov 3, 2016 Congressional and Public Affairs Allie Ryan (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Nov. 3, 2016 – Flavor Trade, LLC., a Kansas City, Mo. establishment, is recalling approximately 113 pounds of beef jerky products that were produced without the benefit of federal inspection and used the USDA mark of inspection without authorization, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The beef jerky items were produced on Sept. 27, Sept. 28, Oct. 25 and Oct. 26, 2016. The following products are subject to recall: View Labels PDF Only http://www.fsis.usda.gov/wps/wcm/connect/53e2ebba-4eea-4cac-b2a7-d0971e1616bf/102-2016-labels.pdf?MOD=AJPERES 3-oz. sealed packages containing “Craft Beer Jerky: Created with Wheat” which may or may not include package code 614261. 3-oz. sealed packages containing “Craft Beer Jerky: Created with Porter” which may or may not include package code 619290. The products subject to recall may or may not incorrectly bear a USDA mark of inspection which would include establishment number “EST. 48135”. These items were shipped to retail locations in Missouri. The problem was discovered by FSIS inspection personnel after a consumer provided a package of the product. There have been no confirmed reports of illness or adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls. Consumers with questions about the recall can contact Shannon Kimball, Owner, at (816) 531-2288. Media with questions about the recall can contact David Eckert, Sales Manager, at (816) 668-7493. John
  17. http://www.fda.gov/Safety/Recalls/ucm527875.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. AC Creamery Inc. Recalls "Manila Sky Purple Yumm Ice Cream" Because Of Possible Health Risk For Immediate Release November 2, 2016 Contact Consumers 714-871-9951 Media Susan Brown 714-871-9951 Announcement View Product Photos http://www.fda.gov/Safety/Recalls/ucm527875.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery#recall-photos AC Creamery Inc. of Anaheim, CA, is recalling its 16 ounce packages of "Manila Sky Purple Yumm Ice Cream" because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. The recalled “Manila Sky Purple Yumm Ice Cream" were distributed nationwide in retail stores and events such as; Florida Food & Lodging Show, Festival of Philippine Arts & Culture and California State University Pilipino American Student Association (CSUF PASA) Friendship Games The product comes in a 16 ounce, paper cup marked with an expiration date of Mar 06, 2018 stamped on the bottom. No illnesses have been reported to date in connection with this problem. The U.S. Food and Drug Administration (FDA) found samples positive for Listeria monocytogenes in the contract manufacturer’s, Dr. Bob’s of Upland, LLC, facility, and in finished product of another company’s brand, leading the contract manufacturer to recall all ice cream products produced this year. Consumers who have purchased 16 ounce packages of "Manila Sky Purple Yumm Ice Cream" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-714-871-9951, Mondays-Fridays from 9AM -5PM Pacific Time. John
  18. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-100-2016-release News Release Crider Inc. Recalls Canned Organic Roasted Chicken Breast Due to Possible Foreign Matter Contamination Class I Recall 100-2016 Health Risk: High Oct 25, 2016 Distribution List PDF http://www.fsis.usda.gov/wps/wcm/connect/43c5aea4-2d67-46f9-b31c-29e55676876f/RC-100-2016-Retail-List.pdf?MOD=AJPERES&CONVERT_TO=url&CACHEID=43c5aea4-2d67-46f9-b31c-29e55676876f Congressional and Public Affairs Jeremy J. Emmert (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Oct. 25, 2016 – Crider Inc., a Stillmore, Ga., establishment, is recalling approximately 5,610 pounds of canned Organic Roasted Chicken Breast that may be contaminated with foreign materials the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The cans of Wild Planet Organic Roasted Chicken Breast were produced on January 16, 2016. The following products are subject to recall: View Label PDF only http://www.fsis.usda.gov/wps/wcm/connect/6d92e296-fbba-4a80-a715-4132e514264f/100-2016-labels.pdf?MOD=AJPERES 1,496 cases of 5 ounce cans of “Wild Planet Organic Roasted Chicken Breast – 100% Chicken Breast & Sea Salt – No Liquids Added” with a Best Buy Date of 01/16/18 The products subject to recall bear establishment number “EST. 31812” inside the USDA mark of inspection. These items were shipped to multiple distributers for further distribution. The problem was discovered when a distributer received two complaints from consumers involving foreign matter in the product on October 2, 2016 and October 9, 2016. The company received a report of a potential injury associated with consumption of this product. FSIS has received no additional reports of injury or illness from consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls. Media with questions about the recall can contact Mark Howell, Vice President of Sales, at (912) 562-9276. Customer with questions about the recall can contact Judy Tridico, Customer Service representative at (912) 562-9162 John
  19. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-086-2016-release News Release RFG Canada Inc. Recalls Meat and Poultry Pizza Products Distributed Without Benefit of Import Inspection Class I Recall 086-2016 Health Risk: High Sep 22, 2016 Distribution List PDF http://www.fsis.usda.gov/wps/wcm/connect/a3fd7b92-6831-47ec-a990-8887845d64f3/RC-086-2016-Retail-List.pdf?MOD=AJPERES&CONVERT_TO=url&CACHEID=a3fd7b92-6831-47ec-a990-8887845d64f3 Congressional and Public Affairs Benjamin A. Bell (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Sept. 22, 2016 – RFG Canada Inc., a Toronto, Ontario establishment, is recalling approximately 1,250 pounds of meat and poultry pizza products imported from Canada and not presented to FSIS for re-inspection upon entry to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Without the benefit of full inspection, a possibility of adverse health consequences exists. The self-rising chicken bacon ranch and thin crust pepperoni pizzas were produced in Canada on March 3 and August 17, 2016 and imported to the United States on/around Sept. 13, 2016. The following products are subject to recall: View Labels PDF Only http://www.fsis.usda.gov/wps/wcm/connect/e0199bbd-5f92-462d-85bc-54872e977838/086-2016.pdf?MOD=AJPERES 30.3 oz. packages of “WEIS Self-Rising Pizza; Chicken Bacon Ranch” containing the UPC code 041497028337 and Canada Establishment 411 and best by date MAY 16 2017. 20.2 oz. packages of “WEIS Thin Crust Pepperoni Pizza 3 Pack” containing the UPC code 041497026524 and Canada Establishment 411 and best by date DEC 01 2016. The products subject to recall bear establishment number “Canada Est. 411.” These items were shipped to retail locations in Maryland, New York, and Pennsylvania. The problem was discovered on Sept. 16, 2016, by the FSIS import inspector during routine monitoring of shipments destined for their assignment. On Sept. 20, 2016, FSIS confirmed that there was a failure to present shipment and the products were already in commerce without receiving FSIS re-inspection upon entry to the United States. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls. Consumers and media with questions about the recall can contact Joe Ricci, Chief Executive Officer, at (416) 798-9900 ext. 221. John
  20. https://cpsc.gov/Recalls/2017/Kikkerland-Design-Recalls-Teapots-with-Stands-Due-to-Fire-Hazard Kikkerland Design Recalls Teapots with Stands Due to Fire Hazard Recall date: November 1, 2016 Recall number: 17-023 Recall Summary Name of product: Kikkerland and Cost Plus World Market brand teapots with bamboo stands Hazard: The bamboo votive stand can catch fire, posing a fire hazard to consumers. Remedy: Refund Consumer Contact: Kikkerland at 800-727-7151 from 9 a.m. to 5 p.m. ET Monday through Friday or online at www.kikkerland.com. Recall Details Units: About 7,300 Description: This recall involves Kikkerland and Cost Plus World Market brand teapots with bamboo stands. The 30-ounce glass teapots have a removable glass tea infuser sold with a votive-candle holder inside the bamboo stand. The Kikkerland teapots have model number TP02 printed on the packaging next to the UPC code. The Cost Plus World Market teapots have a white sticker with number 25024784 printed on the packaging. No votive candles were included with the teapots. Incidents/Injuries: The firm has received six reports of the votive stands burning. No injuries have been reported. Remedy: Consumers should immediately stop using the recalled teapots and stands and contact the firm for return instructions. Consumers who purchased online will be mailed instructions on how to receive a refund. Consumers who bought the teapots at stores can return the teapots and stands for a full refund. Sold At: Amazon retailers, Cost Plus World Market, Uncommon Goods and Urban Outfitters and online at www.Amazon.com from March 2014 through September 2016 for between $40 and $70. Importer(s): Kikkerland Design Inc., of New York Manufactured In: China John
  21. https://cpsc.gov/Recalls/2017/Fox-Factory-Recalls-Mountain-Bike-Shock-Absorbers-Due-to-Fall-and-Injury-Hazards Fox Factory Recalls Mountain Bike Shock Absorbers Due to Fall and Injury Hazards Recall date: November 1, 2016 Recall number: 17-022 Recall Summary Name of product: Mountain bike rear shock absorbers Hazard: The bicycle’s rear shock absorber outer sleeve can rupture, allowing the sleeve to come in contact with other bicycle parts or the rider, posing a fall and injury hazard. Remedy: Repair Consumer Contact: Fox toll-free at 855-360-3488 from 8 a.m. to 5 p.m. PT Monday through Friday, email at recall@ridefox.com or online at http://ridefox.com/recall and click on the recall link for more information. Recall Details In Conjunction With: Canadian Flag Units: About 6,100 (in addition, about 1,200 were sold in Canada) Description: This recall involves all model year 2016 and some 2017 FLOAT X2 bicycle rear shock absorbers sold both individually and installed on YT, Giant, Pivot, Intense, Ibis, Scott, Trek, GT, Knolly, Norco, Rocky Mountain, Diamondback, Morpheus, Foes Racing, Orbea and Canyon full-suspension mountain bikes and frames. The solid black or black and gold FLOAT X2 shocks have an air sleeve construction. FLOAT X2 is printed on the external reservoir connected to the blue compression and red rebound adjusters that have X2 and RVS laser etched on them. Recalled shocks do not have a “250 psi max” label directly under the air fill boss on the outer sleeve of the shock. Recalled shocks and bike models can be identified at http://ridefox.com/recall. Incidents/Injuries: The firm has received seven reports of the shock absorber outer sleeve rupturing. No injuries have been reported. Remedy: Consumers should immediately stop using bicycles with the recalled rear shock absorbers and return them to the place of purchase for a free repair. Consumers unable to return their bicycles should contact Fox for instructions on receiving a free repair. Sold At: Independent bike stores nationwide, online at Jenson USA, Pro Bike Supply, Universal Cycles, Go-ride.com and other online bike retailers from March 2015 through September 2016. The shocks were installed as original equipment on full-suspension mountain bikes and frames sold for between about $2,700 to $10,000 and sold individually as an aftermarket accessory for about $600. Manufacturer(s): Fox Factory, Watsonville, Calif. Manufactured In: United States John
  22. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-099-2016-release News Release St. Clair Foods, Inc. Recalls Poultry Products Due To Misbranding And An Undeclared Allergen Class I Recall 099-2016 Health Risk: High Oct 21, 2016 Distribution List PDF http://www.fsis.usda.gov/wps/wcm/connect/f93029fe-e17d-4bd4-9a7f-940b3845fd7c/RC-099-2016-Retail-List.pdf?MOD=AJPERES&CONVERT_TO=url&CACHEID=f93029fe-e17d-4bd4-9a7f-940b3845fd7c Congressional and Public Affairs Benjamin Bell (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Oct. 21, 2016 – St. Clair Foods, Inc., a Memphis, Tenn. establishment, is recalling approximately 26,800 pounds of chicken and dumplings due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain milk, a known allergen, which was not declared on the product label. The chicken and dumplings were produced on various dates from Sept. 13 through Oct. 6, 2016. The following products are subject to recall: View Labels PDF Only http://www.fsis.usda.gov/wps/wcm/connect/407d3c16-93ab-4c58-bfcd-fe5abd560cf2/099-2016-labels.pdf?MOD=AJPERES 5-lb. Plastic sealed packages containing “ST. CLAIR FOODS CHICKEN AND DUMPLINGS” bearing package codes 16257, 16264, and 16280. 2-lb. Plastic sealed packages containing “ST. CLAIR FOODS CHICKEN AND DUMPLINGS” bearing package codes 16257, 16264, and 16280. 5-lb. Plastic sealed packages containing “RON’S HOMESTYLE FOODS CHICKEN AND DUMPLINGS” bearing package codes 16280, 16272, 16264, and 16257. The products subject to recall bear establishment number “EST-6568” inside the USDA mark of inspection. These items were shipped to food service warehouses and distributed for institutional use in Alabama, Arkansas, Kentucky, Mississippi, Tennessee, and Texas. The problem was discovered by the establishment on October 20, 2016 during a review of product specifications. The establishment was not notified by their ingredient supplier that there was a change in the dumpling ingredients to include the addition of the milk ingredient. The establishment immediately notified FSIS that the undeclared milk allergen ingredient was incorporated into their products. There have been no confirmed reports of injury, illness, or adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls. Consumers with questions about the recall can contact Monica Woodruff at (901) 322-7301. Media with questions about the recall can contact Brian Edmonds at (901) 322-7328. John
  23. http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-099-2016-release News Release St. Clair Foods, Inc. Recalls Poultry Products Due To Misbranding And An Undeclared Allergen Class I Recall 099-2016 Health Risk: High Oct 21, 2016 Distribution List PDF http://www.fsis.usda.gov/wps/wcm/connect/f93029fe-e17d-4bd4-9a7f-940b3845fd7c/RC-099-2016-Retail-List.pdf?MOD=AJPERES&CONVERT_TO=url&CACHEID=f93029fe-e17d-4bd4-9a7f-940b3845fd7c Congressional and Public Affairs Benjamin Bell (202) 720-9113 Press@fsis.usda.gov WASHINGTON, Oct. 21, 2016 – St. Clair Foods, Inc., a Memphis, Tenn. establishment, is recalling approximately 26,800 pounds of chicken and dumplings due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain milk, a known allergen, which was not declared on the product label. The chicken and dumplings were produced on various dates from Sept. 13 through Oct. 6, 2016. The following products are subject to recall: View Labels PDF Only http://www.fsis.usda.gov/wps/wcm/connect/407d3c16-93ab-4c58-bfcd-fe5abd560cf2/099-2016-labels.pdf?MOD=AJPERES 5-lb. Plastic sealed packages containing “ST. CLAIR FOODS CHICKEN AND DUMPLINGS” bearing package codes 16257, 16264, and 16280. 2-lb. Plastic sealed packages containing “ST. CLAIR FOODS CHICKEN AND DUMPLINGS” bearing package codes 16257, 16264, and 16280. 5-lb. Plastic sealed packages containing “RON’S HOMESTYLE FOODS CHICKEN AND DUMPLINGS” bearing package codes 16280, 16272, 16264, and 16257. The products subject to recall bear establishment number “EST-6568” inside the USDA mark of inspection. These items were shipped to food service warehouses and distributed for institutional use in Alabama, Arkansas, Kentucky, Mississippi, Tennessee, and Texas. The problem was discovered by the establishment on October 20, 2016 during a review of product specifications. The establishment was not notified by their ingredient supplier that there was a change in the dumpling ingredients to include the addition of the milk ingredient. The establishment immediately notified FSIS that the undeclared milk allergen ingredient was incorporated into their products. There have been no confirmed reports of injury, illness, or adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls. Consumers with questions about the recall can contact Monica Woodruff at (901) 322-7301. Media with questions about the recall can contact Brian Edmonds at (901) 322-7328. John
  24. Own or lease a VW or Audi 2.0 liter diesel car? Here’s what you should know: Because of emissions violations, Volkswagen has been ordered to provide up to $10 billion to owners and lessees of a 2009 to 2015 VW TDI Beetle, Golf, Jetta, Passat or Audi TDI A3. Find important tips from the Federal Trade Commission (FTC) on the settlement program and how to submit a claim. https://www.consumer.ftc.gov/blog/vw-buybacks-and-lease-terminations-begin?utm_campaign=%2B+Money+and+Shopping&utm_source=hs_email&utm_medium=email&utm_content=36765920&_hsenc=p2ANqtz-98E2FjRjrjlT_FlCMNLCYj2pFqcCeYtDyvXjiW8Nq2DZjP8KZ6XOyAw3nJQhMdbnS5R7JC6As50Cj2qWawBXsmpCYFFQ&_hsmi=36765920 Learn how to file a consumer complaint at USA.gov. https://www.usa.gov/consumer-complaints?utm_campaign=%2B+Money+and+Shopping&utm_source=hs_email&utm_medium=email&utm_content=36765920&_hsenc=p2ANqtz-8ajBUiayEXas6_frLiOqooVgIDhF-inGaNL6mLqk7ABPZP33BMvTdNISRyFTg1esbRuWTxAO9aYvJwZmhlVYKDbzYc-w&_hsmi=36765920 John
  25. http://www.emergencyemail.org/newsemergency/anmviewer.asp?a=6825&z=63 RECALL: Chairs H-E-B Recalls Star Chairs Due to Fall Hazard Recall date: October 26, 2016 Recall Summary Name of product: Brazos Embossed Star Chairs Hazard: Weld defects can cause the armrest to detach from base, posing a fall hazard to consumers. Remedy: Refund Consumer Contact: H-E-B at 800-432-3113 between 8 a.m. and 5 p.m. CT Monday through Friday or online at www.heb.com and click on "Recalls" for more information. Recall Details Units: About 600 Description: This recall involves Brazos Embossed star chairs that are brown metal with welded construction and an embossed star design on the back of the chair. The white hangtag on this item has the following product identification: UPC number 8502430906 and item code number 194781. The chair measures 24 inches wide and 33.5 inches in height. Incidents/Injuries: H-E-B has received one report of the armrest detaching from the base. No injuries have been reported. Remedy: Consumers should immediately stop using the recalled chair and return it to the store where purchased for a full refund. Sold Exclusively At: H-E-B stores in Texas from February 2016 through September 2016 for about $60. Importer(s): Parkway Manufacturing and Trading Company, of San Antonio, Texas Distributor(s): Parkway Manufacturing and Trading Company, of San Antonio, Texas Manufactured In: China John
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