Ukrop’s Homestyle Foods, a Richmond, Va., establishment, is recalling approximately 22,880 pounds of baked spaghetti and chicken cobbler products that may be contaminated with foreign material, specifically metal slivers, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced.
Boticelli Foods Recalls Bettergoods Pistachio Nut Butter Sold at Walmart Because of Possible Health Risk
Boticelli Foods of Melville NY, is recalling 1 lot of bettergoods Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961, Lot LB028ACP04, sold at Walmart, because it has the potential to be contaminated with Salmonella,
The U.S. Food and Drug Administration (FDA) announced a recall on approximately 11,960,623 bottles of eye drops sold nationwide.1 This is due to sterility concerns.
The products being recalled are nine types of Rohto Cooling Eye Drops sold at retail locations across the U.S. Distributed by The Mentholatum Company, the following eye drops are affected, including impacted UPCs, lot codes and expiration dates:
American Regent, Inc. Animal Health Issues Nationwide Recall of Two Lots of Adequan® Canine and Two Lots of Adequan® I.M. Due to Visible Glass Fiber Material in the Product
FOR IMMEDIATE RELEASE – July 31, 2026 – Shirley, NY, American Regent, Inc. Animal Health is conducting a nationwide recall of two lots (25011 and 3369) of Adequan® Canine Injection (for dogs), 100 mg/mL 5mL multi-dose vials and two lots (24416 and 25265P) of Adequan® i.m. Injection (for horses), 500mg/5 mL single-dose 5mL vials to the consumer level. The products are being recalled due to the presence of glass fibers found during testing of internally retained samples.
FDA announces highest recall for certain ventilators, introducer kits | AHA News American Hospital Association The Food and Drug Administration has identified Class I recalls of two products: certain Astral ventilators by Resmed due to a supercapacitor that …
BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
FRANKLIN LAKES, N.J. (July 31, 2026) – BD (Becton, Dickinson and Company) is voluntarily recalling specific lots of BD® Intraosseous Vascular Access System Needle Sets to the user level. These products are being recalled following reports that some users experienced difficulty removing the obturator (stylet) after placement of the needle set. Based on complaint reports, bench testing completed by BD and clinical observations, this may occur if the drill is not pulled straight back during insertion or if the obturator is incorrectly rotated during removal.
