Freshway Foods is voluntarily recalling 6,671 pounds of sliced apples that were packaged on November 12 using the same packaging machine, which may have been contaminated with Listeria monocytogenes. A table of recalled consumer packproducts, their respective use-by-dates and the states to which the company shipped them is provided below.
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FDA expands Zytiga’s use for late-stage prostate cancer
The U.S. Food and Drug Administration today expanded the approved use of Zytiga (abiraterone acetate) to treat men with late-stage (metastatic) castration-resistant prostate cancer prior to receiving chemotherapy.
Sugar Flowers Plus Inc Issues Allergy Alert on Undeclared Egg White in Cake Decors Pastillage (gumpaste) Flowers
Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage (gumpaste) Flowers because of the undeclared use of egg white wash as a “glue” for the inner petals of flowers. People who have an allergy or severe sensitivity to egg whites run the risk of life threatening allergic reaction, anaphylaxis, that requires immediate medical care if they consume the entire product.
LifeVantage Corporation Announces Voluntary Recall and Replacement of Select Lots of Protandim® Dietary Supplement Due to Potential Health Risk
December 5, 2012 – SALT LAKE CITY, (GLOBE NEWSWIRE) – LifeVantage Corporation (NASDAQ: LFVN) announced today that it is contacting affected independent distributors and other customers to voluntarily recall and replace bottles of its Protandim®, the Nrf2 Synergizer®, dietary supplement from the lots shown below. The Company is taking this action due to the possible inclusion of small metal fragments in the final product.
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Qualitest Issues Voluntary, Nationwide Recall of 101 Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, Usp 10 Mg/500 Mg Due to the Potential for Oversized Tablets
Qualitest, a subsidiary of Endo Health Solutions, (Nasdaq: ENDP) today issued a voluntary nationwide recall for 101 lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg. This includes product with the following NDC numbers and lot numbers beginning with the letter “C”.
FDA warns consumers not to feed certain Nature’s Deli Chicken Jerky Dog Treats
• The FDA is warning consumers not to feed their pets certain Nature’s Deli Chicken Jerky Dog Treats packaged and distributed by Kasel Associates Industries Inc. (Kasel) with a lot code of BESTBY061913DEN. The company has declined to perform a voluntary recall at this time.
Bunnell Incorporated Issues Nationwide Recall Notification of Life Pulse High-Frequency Ventilator Patient Circuits
On December 12, 2012 Bunnell Incorporated will voluntarily initiate a nationwide recall notification of Life Pulse High-Frequency Ventilator Patient Circuits.
Price Chopper Supermarkets Recalls Central Market Classic Cinnamon Coffee Cake Purchased At Mountain Road Store In Worcester, MA
October 21, 2012 -(Schenectady, N.Y.) –Price Chopper Supermarkets is issuing a voluntary recall on certain Cinnamon Nut Coffee Cakes purchased only at the Mountain Rd. store in Worcester, MA, because they were incorrectly
labeled as Pumpkin Coffee Cakes and therefore did not list tree nuts as an ingredient. The cakes were purchased at the Mountain Road store only (located at 72 Pullman St. in Worcester), were purchased after
October 11, 2012 and would have an expiration date between October 17 and October 25.
Stop & Shop alerts customers to voluntary recall of
The Stop & Shop Supermarket Company LLC, following a recall by Veggie Patch, announced it removed from sale packages of ultimate meatless burgers due to possible contamination by listeria monocytogenes. The following product is included in this recall: Veggie Patch Ultimate Meatless Burger, UPC 61012900211, 9 oz., sell by date of January 12, 2013 Stop & Shop has received no reports of illnesses to date.
FDA announces public-private partnership to develop regulatory science that will speed patient access to new medical device technologies
The U.S. Food and Drug Administration announced today that it is part of the first public-private partnership to promote medical device regulatory science with a focus on speeding the development, assessment, and review of new medical devices.