Good Seed Inc. of Springfield, VA is voluntarily recalling all packages of soybean sprouts and mung bean sprouts because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals 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.
NORTHWEST FARM FOOD COOPERATIVE VOLUNTARILY RECALLS FROZEN RAW CAT FOOD DUE TO POSSIBLE SALMONELLA CONTAMINATION
Northwest Farm Food Cooperative of Burlington, WA, is voluntarily recalling frozen raw Cat Food with the code Jul12015B due to their potential to be contaminated with Salmonella.
Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products.
Kent, Washington Firm Issues Allergy Alert On Undeclared Peanut Ingredients
Real Foods of Seattle, LLC of Kent, WA is recalling 29 cases of Harvest Slaw Kit and 13 cases of Broccoli Salad Kit because it may contain undeclared peanut ingredients. No other products are impacted by this recall. This recall is being conducted in coordination with the U.S. Food and Drug Administration (FDA). People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Blue Square Market Issues Voluntary Nationwide Recall of Kaboom Action Strips and Lida Daidaihua Due to the Presence Of Undeclared Sulfoaildenafil, Sibutramine And Phenolphthalein
Blue Square Market Inc. of North Huntingdon, PA, is recalling “Kaboom Actions Strip 12 Pack” and LiDa DaiDaiHua to the user level after FDA analysis revealed the products contain undeclared active pharmaceutical ingredients. Kaboom was found to contain sulfoaildenafil and LiDa DaiDaiHua was found to contain sibutramine and phenolphthalein. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 due to increased risk of heart attacks and strokes. Phenolphthalein is an ingredient previously used in over-the-counter laxatives, but because of concerns of carcinogenicity, it is not currently approved for marketing in the United States.
Mahina Mele Farm Recalls Their Macadamia Nut Products Due to Possible Health Risk
Mahina Mele Farms is recalling the following products after FDA testing found Salmonella in macadamia nuts. Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Angry Orchard Cider Company Announces Voluntary Recall of Select Cases of Angry Orchard Crisp Apple Hard Cider
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.
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).