Browse through 1,551 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
Amy's Kitchen recalled 38,856 frozen Bean & Rice Burritos on October 2, 2025. The recall follows concerns about potential contamination with foreign objects. Consumers should not consume the product and seek refunds immediately.
Leprino Foods recalled over 5.4 million pounds of mozzarella cheese on October 2, 2025, due to possible stainless steel contamination. The recall affects products distributed in Ohio, Tennessee, Texas, Utah, and Wisconsin. Consumers should not consume the product and should seek a refund.
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.
ICU Medical recalled 23,203 IV administration sets on October 2, 2025. The sets lack an internal shutoff valve, risking fluid over-delivery and air infusion. This recall affects devices distributed worldwide, including the U.S., Canada, Australia, and New Zealand.
Church & Dwight Co., Inc. recalled 21,912 bottles of ZICAM Medicated Fruit Drops on October 1, 2025. The recall stems from a labeling mix-up that failed to disclose elderberry as an ingredient. Consumers should stop using the product immediately.
Camber Pharmaceuticals, Inc. recalled Ketorolac Tromethamine Injection on October 1, 2025. The recall affects a specific lot due to the presence of glass particles. This recall pertains to the 60 mg/2 mL single-dose vials distributed nationwide.
Demers Food Group recalled 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine on October 1, 2025. The product may contain linguine linked to Listeria monocytogenes. Consumers should not consume it and seek a refund.
Abiomed issued a recall for 10,153 Automated Impella Controllers on October 1, 2025. The devices face potential cybersecurity vulnerabilities related to their operating system. Healthcare providers and patients should stop using these devices immediately.
B BRAUN MEDICAL recalled 1,298,454 hemodialysis bloodlines on September 30, 2025. The recall results from the risk of micro-air bubbles due to damaged connectors. Patients should stop using the product immediately and follow the manufacturer’s instructions.
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.
Oceans Kitchen recalled 496 cases of imitation crabmeat on September 30, 2025. The product may contain Clostridium botulinum due to temperature abuse during storage. Consumers should not consume the product and seek refunds.
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.
New Age International, Inc. recalled 175 boxes of its Signature brand Enoki Mushroom on September 29, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not eat the product and seek a refund or replacement.
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.
Acella Pharmaceuticals recalled 4,680 bottles of Doxycycline Hyclate Tablets on September 29, 2025. The recall follows failed dissolution specifications, which can affect medication efficacy. This recall includes 500-count bottles distributed nationwide in the USA.
AFCO recalled hand sanitizer on September 29, 2025, due to a risk of methanol contamination. The company failed to conduct required testing on incoming alcohol components. Consumers should stop using the product immediately.
Acuity Specialty Products recalled its Wyandotte Sanifect E3 hand sanitizer on September 29, 2025. The recall affects multiple package configurations due to potential methanol contamination. Consumers should stop using the product immediately and contact the company for guidance.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 x-ray systems on September 29, 2025. The devices may suffer from corrosion of the Image Intensifier Television control board, leading to poor image quality. Users must stop using the device immediately and follow the recall instructions.