269 recalls tagged with “metal”.
Amy's Kitchen recalled 38,856 frozen Gluten Free Bean & Rice Burritos across 3,238 cases distributed to 21 states on Oct. 2, 2025. The recall cites potential contamination with foreign objects. Consumers should not eat the product and should contact Amy's Kitchen for refund or replacement information.
Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.
AFCO's hand sanitizer 5515 is being recalled nationwide through distributors and retailers. The recall cites cGMP deviations that left methanol risk unexcluded. Consumers and healthcare providers should stop using this product immediately and contact Acuity Specialty Products for guidance.
Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.
Wise Wife Ground Cinnamon from SLR Food Distribution is recalled across New York, Minnesota, Florida, Oklahoma and Ohio. Elevate lead levels were detected in the product. Consumers should not consume it and should contact SLR Food Distribution for refund or replacement.
Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.
Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix due to potential Listeria monocytogenes contamination. The product was packed by WPS in Minneapolis, MN and distributed to five Midwest states. Consumers should not eat the recalled fruit and should contact the distributor for refund or replacement.
Synthes (USA) Products LLC recalled 120 low-profile locking screws for intramedullary nails used in the RFN-Advanced Retrograde Femoral Nailing System and the Tibial Nail Advanced System. The recall covers devices distributed worldwide through healthcare providers. The external packaging mislabels screw lengths: 42 mm screws are labeled 46 mm and 46 mm screws are labeled 42 mm. Hospitals and spine
Georgia Nut Co recalls 170,993 cases of tru fru Dark + White Chocolate Freeze-Dried Strawberries sold nationwide after metal fragments were detected. The recall covers 1.7oz, 3.4oz, and 13oz pouches with UPCs 850048358331, 850048358270, and 850048358379 and distributions to major retailers including Albertsons, CVS, Kroger and Target. Consumers should not eat the product and should await a recall‑
Georgia Nut Co recalls 76,121 cases of tru fru Strawberries + Creme Freeze-Dried Fresh 3.4 oz pouches sold nationwide at retailers including Albertsons, CVS, Food Lion, H-E-B, Kroger, Target, Stew Leonard's and more. A potential for metal fragments in some packages is the hazard. Consumers should stop using the product and contact Georgia Nut Co for a refund or replacement.
Volkswagen Group of America recalls one 2025 Audi SQ7 over a potential fuel leak from an improperly tightened high pressure fuel pump. The recall affects a single vehicle and is classified as high risk due to fire potential. Owners should contact Volkswagen for inspection and repair at no cost.
Audi and Volkswagen Group of America recall 2025 GTI, Golf R, Audi A5, A6 Sportback E-Tron, S5, S6 Sportback E-Tron, 2026 Q4 Sportback E-Tron and Q4 E-Tron vehicles. The torsion bar in the front seat belt retractors may be damaged during production. Dealers will replace one or both front seat belts at no charge. VIN lookups begin Sept 26, 2025 and owner letters go out Nov 21, 2025.
Biomet recalled 98 ZipTight Acute AC Joint Implant Single Ziploop devices on Sept. 23, 2025. A missing slotted button assembly was identified in one lot. Healthcare providers and patients should stop using the device immediately and follow Biomet’s recall instructions.
BD MAX System recall affects 62 units distributed worldwide in 2025 after unauthorized access to service credentials. An unauthorized actor accessed credentials used by BD technical support teams. Healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.
BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.
Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.
EnHomee recalled Fabric 13-Drawer Dressers sold directly by EnHomee Direct due to a tip-over and entrapment hazard. The units do not meet the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and seek a full refund.
Taproom Gourmet bulk Empire Mix recall affects 3,547 cases distributed across New York, New Jersey, Connecticut, California, Illinois and Florida. The product lacks an ingredient label and contains undeclared allergens. Consumers should not consume the product and should seek a refund or replacement from Egress Capital Partners.
Cardinal Health 200, LLC recalled Salem Sump PVC Tubes worldwide after ARV breakage complaints. The anti-reflux valve can break under excessive force during use. Clinicians and patients should stop using the device and await recall instructions.