Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Almpal recalls its dissolved oxygen test kits sold on Amazon after authorities found the sulfuric acid inside the kit lacked required child-resistant packaging. The recall is active as of Oct 2, 2025. Consumers should stop using the kit and follow disposal and refund instructions from the seller.
Zyntony recalled Kogalla power banks sold on Kogalla.com due to fire and burn hazards. The recall targets BP125, BatPak 2F and BatPak 3F models. The lithium-ion batteries can overheat and ignite, even when not in use. Consumers should stop using the recalled power banks and contact Kogalla for a free replacement.
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.
ICU Medical recalls 23,203 IV gravity burette sets worldwide. The burette component is missing an internal shutoff valve, which can delay therapy, cause overdelivery, or allow air to be infused. Stop using the device and contact ICU Medical for instructions.
Giant Eagle recalled 486.65 pounds of Smoked Mozzarella Penne Salad on October 2, 2025. The recall follows potential listeria contamination. The affected product was distributed in Pennsylvania, Ohio, Indiana, and Maryland.
Leprino Foods recalled 5,453,442 pounds of LMPS bulk mozzarella distributed to Ohio, Tennessee, Texas, Utah and Wisconsin after the FDA enforcement notice. The recall cites the possible presence of stainless steel pieces in the product. Consumers should not consume the mozzarella and should contact Leprino Foods for refund or replacement information.
Giant Eagle recalled 27 pounds of Smoked Mozzarella Penne Salad on October 2, 2025, due to potential listeria contamination. The product was sold in Pennsylvania, Ohio, Indiana, and Maryland. Consumers should not consume the salad and should seek a refund or replacement.
Giant Eagle recalled 16 pounds of Smoked Mozzarella Penne Salad on October 2, 2025, due to potential listeria contamination. The affected product was sold in Pennsylvania, Ohio, Indiana, and Maryland. Consumers should not consume the product and contact the company for refunds.
Church & Dwight recalled 21,912 bottles of ZICAM Cold Remedy Medicated Fruit Drops Elderberry from nationwide distribution in the United States. The label did not indicate elderberry as an ingredient though the product contains elderberry. Consumers should stop using the product and contact Church & Dwight for guidance.
DEMERS FOOD GROUP LLC is recalling Scott & Jon's Shrimp Scampi with Linguine, 9.6 oz, sold nationwide. The linguine component, manufactured by Nate's Fine Foods LLC, was recalled for Listeria monocytogenes and linked to an ongoing outbreak. Consumers should not consume the product and should contact DEMERS FOOD GROUP LLC for refund or replacement using email, fax, letter, press release, telephone,
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.
Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.
B BRAUN MEDICAL recalled 1,298,454 STREAMLINE BLOODLINE SET FOR DIALOG devices nationwide in the United States after observations of micro-air bubbles and air-in-line alarms linked to damaged arterial and venous connectors. The defect increases the risk of air entering the bloodstream during dialysis. Patients and healthcare providers should stop using this device immediately and follow the recall
Ocean's Kitchen recalled 496 cases of imitation crab meat shredded, distributed in Washington state. The product is refrigerated and vacuum-packaged. The recall cites potential contamination with Clostridium botulinum due to temperature abuse during chilled storage. Consumers should not consume the product and should contact Oceans Kitchen for refunds or replacements.
Lunds & Byerly's recalled 744 units of Pecan Caramel Clusters on September 30, 2025. The products may contain undeclared cashews, posing a severe allergy risk. Consumers should not eat the product and seek refunds immediately.
SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.
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.
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.
Wegmans recalled 2,216 units of Ultimate Plain Cheesecake on September 29, 2025. The product contains undeclared pecans, posing a serious allergy risk. Customers in Pennsylvania and Virginia should not consume this item.
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.