2,679 recalls tagged with “immediate action”.
Wegmans Food Markets recalls 521 units of Wegmans 58 oz Ultimate Blueberry Cheesecake sold in Virginia, Maryland, North Carolina and Washington, D.C. The product contains undeclared pecans, creating an allergy risk. Consumers who purchased the cheesecake should not eat it and should contact Wegmans for a refund or replacement.
Sunbeam Products recalled more than 1 million Oster French Door Countertop Ovens after reports of doors closing unexpectedly and causing burn risks. The recall covers four Oster models and affects units sold nationwide. Consumers should stop using the ovens and contact Sunbeam for a free repair kit.
Mad Rabbit recalls RELIEVE lidocaine numbing cream due to non‑compliant packaging that could allow poisoning of young children. The recall covers a product sold under the Mad Rabbit brand and issued on 2025-09-25. The packaging does not meet the Poison Prevention Packaging Act requirement for child resistance. Consumers should stop using the product immediately and contact Mad Rabbit for a free, a
Persilux recalled zebra blinds sold on Amazon after safety hazards were found. The recall cites long operating cords that can cause strangulation and entanglement. The company offers a free repair kit and instructions to remove cords. Consumers should stop using the product immediately and contact Persilux for remedy information.
AMTRADING recalled Hoovy Cooling Gel Insert Pads for car seats and strollers on 2025-09-25. The pads contain an inner cooling layer activated by a child’s weight and can overheat in sun or a hot car. Consumers should stop using the recalled pad immediately and contact AMTRADING for a full refund.
LeMaitre Vascular recalled 1 Artegraft AG1015 vascular graft distributed to Arkansas hospitals after a packaging size labeling error. The packaging error could lead to using the wrong size graft during surgery. Hospitals and patients should stop using the device and follow recall instructions. See the recall letter for instructions from LeMaitre Vascular or your healthcare provider.
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.
DJO recalled 1,594 Cold Form Wraps for back and shoulder use nationwide through multiple retailers. The IFU directs heating in a microwave for 3 minutes, which can cause leaks or seam breaks and temperatures high enough to cause a second-degree burn. Stop using the device and follow the manufacturer’s recall instructions.
Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.
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‑
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.
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.
Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.
Ent ecavir 0.5 mg tablets, distributed nationwide in the United States by Zydus Pharmaceuticals USA Inc., are recalled, affecting 912 bottles. The recall is due to an out-of-specification organic impurity detected in a batch, Class II. Healthcare providers and patients should stop using the product immediately and contact Zydus Pharmaceuticals USA for guidance.
NOW Foods recalled 1,689 10 oz pouches of NOW Real Food Organic Unsalted Whole Raw Cashews nationwide after undeclared pine nuts were detected. The hazard poses an allergen risk. Consumers who bought this product should stop using it and contact NOW Foods for a refund or replacement.
Orwashers brand Soho Sourdough XL Batard is being recalled after labeling errors could hide sesame seeds. The recall covers 4 pallets of 6 pieces per case in Massachusetts. Consumers should avoid consumption and contact Oven Artisans LLC for refunds or replacements.
BD recalled 177 units of the BACTEC Blood Culture System worldwide after an unauthorized actor accessed product service credentials. The breach could allow unauthorized access to system configurations and data. Healthcare facilities should stop using the affected equipment and follow BD’s recall instructions.
Southwind Foods LLC dba Great American Seafood Imports Co. expanded recall covers Arctic Shores, Best Yet, Great American and Master Catch frozen shrimp sold nationwide by multiple retailers after Cesium-137 contamination was detected. The contaminated product was manufactured under insanitary conditions. Consumers should not eat the product and should contact the company for refunds or replaced.
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 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.