This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program Read More (external link)...
Continue readingThis communication is part of the Communications Pilot to Enhance the Medical Device Recall Program Read More (external link)...
Continue readingDessert Holdings LLC is recalling Target brand Favorite Day™ Gourmet New York Style Cheesecake 6oz/2ct, Lot code 25028A1 000039133 UPC 0 85239 09690 1 due to product mislabeling resulting in undeclared pecans. People who have an allergy or severe sensitivity to pecans run the risk of serious or life Read More (external link)...
Continue readingA manufacturing error may cause ProPort Plastic Implantable Ports, which are used in patients who need repeat venous access for treatment, to separate before, during, or after implantation. Read More (external link)...
Continue readingPipeline Vantage Embolization Devices block off blood flow to intracranial aneurysms. Some devices do not attach properly or fail to stay attached. Read More (external link)...
Continue readingARLINGTON, VA., March 17, 2025 — Nestlé USA is initiating a voluntary recall of a limited quantity of Lean Cuisine® and STOUFFER’S® frozen meals due to the potential presence of wood-like material. Read More (external link)...
Continue readingSavage Pet of El Cajon, CA is recalling 66 Large Chicken Boxes 84 oz. and 74 Small Chicken Boxes 21 oz. with the lot code/best by date of 11152026 because it has the potential to contain H5N1, also known as bird flu. Read More (external link)...
Continue readingSeaBear Company of Anacortes, Washington is recalling two variations of seafood chowder (Smoked Salmon Chowder & Alehouse Clam Chowder), because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Read More (external link)...
Continue readingHAR Maspeth Corp, Maspeth NY, is recalling its 8 ounce and 12 ounce packages of "JINGA GLASS NOODLES W/ VEGETABLES (Japche)" because they contain undeclared eggs. Read More (external link)...
Continue readingC.H. Guenther & Son LLC of San Antonio, TX, is recalling its 365 Whole Foods Market Small Bites Macaroni & Cheese because it may contain undeclared eggs and meat ingredients. Read More (external link)...
Continue readingThe FDA is adding hemodialysis bloodlines (also referred to as set, tubing, blood, with and without anti-regurgitation valve; product code FJK) to the Medical Device Shortage List because of recent supplier issues. Read More (external link)...
Continue readingDr. Reddy’s Laboratories Ltd is recalling one Batch/Lot No: A1540076 of Levetiracetam in 0.75% Sodium Chloride Injection, 1,000 mg/100 mL (10 mg/mL) single-dose infusion bags to the consumer level, in the United States. Read More (external link)...
Continue readingOn March 11, 2025, Liaoning Cheng Da USA Inc. of San Gabriel, California is recalling Hot Pot Sauce Because it may contain undeclared peanut, soy, sesame, and wheat. People who have an allergy or severe sensitivity to peanut, soy, sesame, and wheat run the risk of serious or life-threatening allergi Read More (external link)...
Continue readingNew Age International Inc of Brooklyn, NY is recalling all lots of Daily Veggies brand Enoki Mushroom, 200g, Product of Korea, because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people Read More (external link)...
Continue readingAs a precautionary measure, the following lots of Immune Globulin Intravenous (IGIV) and Immune Globulin Subcutaneous (IGSC) have been voluntarily withdrawn by the manufacturers due to a higher rate of allergic/hypersensitivity type reactions, some of which were considered medically significant. Read More (external link)...
Continue readingNew York Wholesale Group of Hicksville, NY is recalling Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka Powder, and Zaarah Herbals Bhringraj Powder to the consumer/user level because it has the potential to be contaminated with elevated levels of lead and arsenic. Read More (external link)...
Continue readingSmiths Medical has issued an Urgent Medical Device Correction to notify affected global customers of a potential issue with the 2.0, 2.5, 3.0 and 3.5 mm sizes of Intubation ORAL/NASAL Endotracheal Tube products being smaller than expected. Read More (external link)...
Continue readingADM Animal Nutrition, a division of ADM (NYSE: ADM), is recalling specific pelleted animal feed products because they may contain elevated levels of copper or have levels of zinc below the represented amounts which could be harmful to cattle. Read More (external link)...
Continue readingThis communication is part of the Communications Pilot to Enhance the Medical Device Recall Program Read More (external link)...
Continue readingThis communication is part of the Communications Pilot to Enhance the Medical Device Recall Program Read More (external link)...
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