Angry Orchard Cider Company, LLC, Cincinnati, Ohio, today announced that it is conducting a voluntary recall of select cases (24/12oz bottles), 12-packs and 6-packs of Angry Orchard Crisp Apple Hard Cider. The precautionary action comes after the Company received inquiries from consumers that had experienced broken bottles or bottles overflowing when opened. After conducting follow-up quality testing, the Company determined that the affected cider is limited to two batches, produced on June 15 and June 29, 2015.
Category Archives: Food & Drug Recalls
Voluntary Nationwide Recall Of A Thousand Virgins Grey Wash Tattoo Inks And Tattoo Kits Due To Microbial Contamination
FOR IMMEDIATE RELEASE – Aug 4, 2015 – A Thousand Virgins Corp. in Miami (City of Industry), FL is recalling all lots of tattoo Inks described below due to microbiological contamination. A Thousand Virgins grey wash inks; G1, G2 and G3, that are labeled with Lot#129, and bearing the expiration date: 1/16, revealed contamination with Mycobacterium chelonae, Microbacterium organisms, and the molds Cryptococcus albidus and members of the Penicillium genus.
Federal judge enters permanent injunction against Wisconsin dietary supplement manufacturers
Three dietary supplement companies, under the same ownership and located in Wautoma, Wisconsin, will not be allowed to manufacture or sell dietary supplement products until FDA has determined that the businesses are in compliance with federal manufacturing regulations and other requirements, according to a federal court order signed Aug. 4, 2015.
FDA acts to stop Sacramento tofu and sprout manufacturer from selling adulterated food
On August 3, 2015, U.S. Magistrate Judge Carolyn K. Delaney in the U.S. District Court for the Eastern District of California entered a consent decree against Henh Wong Fresh Produce, a tofu and sprout manufacturer and distributor, and its owner, current manager, and former manager after the U.S. Food and Drug Administration documented multiple violations of federal food safety laws and regulations. The U.S. Department of Justice sought the consent decree on behalf of the FDA.
Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products
On July 2, 2015, Cook Medical initiated a lot-specific voluntary recall of 2,239 lots of Beacon Tip Angiographic Catheters. Globally, 95,167 devices are subject to this recall. The products include specific versions and lot numbers of the Torcon NB® Advantage Beacon® Tip Catheters (Catalog Prefix HNBR5.0), Royal Flush® Plus Beacon® Tip High-Flow Catheters (Catalog Prefix HNR4.0), and Slip-Cath® Beacon® Tip Catheters (Catalog Prefix SCBR5.0).
Cook Medical Issues Global Recall Of Beacon Tip Angiographic Catheter Products
On July 2, 2015, Cook Medical initiated a lot-specific voluntary recall of 2,239 lots of Beacon Tip Angiographic Catheters. Globally, 95,167 devices are subject to this recall. The products include specific versions and lot numbers of the Torcon NB® Advantage Beacon® Tip Catheters (Catalog Prefix HNBR5.0), Royal Flush® Plus Beacon® Tip High-Flow Catheters (Catalog Prefix HNR4.0), and Slip-Cath® Beacon® Tip Catheters (Catalog Prefix SCBR5.0).
The Kraft Heinz Company Voluntarily Recalls Select Varieties of Kraft Singles Products Due to Potential Choking Hazard
The Kraft Heinz Company is voluntarily recalling select code dates and manufacturing codes of Kraft Singles individually-wrapped slices due to the possibility that a thin strip of the individual packaging film may remain adhered to the slice after the wrapper has been removed. If the film sticks to the slice and is not removed, it could potentially cause a choking hazard.
Unichem Pharmaceuticals (USA), Inc. Issues a Voluntary Nationwide Recall of Hydrochlorothiazide Tablets Due to the Potential Presence of Foreign Tablets
Unichem Pharmaceuticals (USA), Inc. (Unichem) is voluntarily recalling one lot of Hydrochlorothiazide Tablets 25 mg 1000-count bottle to the consumer level. This recall has been initiated as a precautionary measure due to the identification of a Clopidogrel tablet found in a bottle of the product.
Kilwin’s Quality Confections, Inc. Issues Allergy Alert on Undeclared Cashew in Sugar Free Milk Chocolate Caramels
Kilwin’s Quality Confections, Inc., of Petoskey, Michigan, is voluntarily recalling 5 ounce containers of SUGAR FREE Milk Chocolate Caramels because they were incorrectly labeled and may contain undeclared cashew. People who have an allergy or severe sensitivity to cashew run the risk of serious or life-threatening allergic reaction if they consume these incorrectly labeled products.
Whole Foods Market Recalls Coconut Curry Cauliflower Salad in Twenty-one Stores Due to Undeclared Almonds
Whole Foods Market is recalling Coconut Curry Cauliflower Salad sold in twenty-one retail stores in CO, KS, NM, UT, and ID due to undeclared almonds. People who have an allergy or severe sensitivity to almonds run the risk of serious or life threatening allergic reaction if they consume these products.