Progressive Laboratories, Inc., located at 3131 Story Road West, Irving, Texas 75038, USA, is voluntarily recalling Testosterzone, Thyroid Resilience, Xenesta Nuvive Men’s, and Xenesta Nuvive Women’s, because it may contain an undeclared allergen. People who have an allergy or severe sensitivity to milk could run the risk of serious or … [Read more...]

LOTTE Int’l America Corp. located in Los Angeles, CA is recalling its 1.48-ounce packages of "Kancho Choco Biscuit" manufactured by LOTTE Confectionery Co. Ltd. Korea because of findings of small amounts of peanut in the product and no peanut declaration. LOTTE Int’l America Corp discovered this fact through lab test result done by CFIA … [Read more...]

TruPet, LLC of Milford, OH, is voluntarily recalling a limited amount of Treat Me Crunchy Beef Delight, 2.5oz Pet treats because the products have the potential to be contaminated with Salmonella. The recall includes only the product listed below. The following affected "Treat Me Crunchy Beef Delight" products were distributed in the continental … [Read more...]

Northwest Naturals of Portland, Oregon is recalling 5lb frozen Chicken and Salmon petfood chubs because it has the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed … [Read more...]

La Pasta Inc. of Silver Spring, Maryland is recalling the private label Potato Gnocchi manufactured for Heinen’s supermarkets because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product. Product was distributed … [Read more...]

Bella All Natural is voluntarily recalling its Diet Capsules labeled as Bella, Lot Number MFD:10.15.2017 EXP: 10.14.2019, to the consumer level. This recall has been initiated due to presence of sibutramine. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market in October 2010 due to safety concerns. N-Desmethyl … [Read more...]

Hospira, Inc., a Pfizer company, is voluntarily recalling 3 lots of Labetalol Hydrochloride Injection, USP, 100 mg/20 mL Vial (NDC 0409-2267-20), and one lot of Labetalol Hydrochloride Injection, USP, Novaplus® (NDC 0409-2267-25) to the hospital/institution level. Hospira, Inc. initiated this recall due to the discovery of cracks on the rim … [Read more...]