Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
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.
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.
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
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.
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider 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.
New Age International recalled 175 boxes of Signature brand Enoki Mushroom sold in New York after testing revealed possible Listeria monocytogenes contamination. The product may be contaminated with Listeria monocytogenes. Consumers who bought it should not eat it and should contact New Age International for refund or replacement information.
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.
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.
Acella Pharmaceuticals recalls doxycycline hyclate tablets, 100 mg, 500-count bottles distributed nationwide in the USA. Stability testing found the lot did not meet dissolution specifications. Consumers and healthcare providers should stop using the product immediately and contact Acella for guidance.
Vicky IT recalled 10 pounds of Bona Fish distributed in New York after FDA enforcement flagged the product for serious safety hazards. The recall cites un-eviscerated fish that may be contaminated with Clostridia botulinum, along with mold and insect larvae. Consumers who bought Bona Fish should not consume it and should contact Vicky IT for a refund or replacement.
Wegmans Food Markets is recalling 521 units of Wegmans Large Ultimate Plain Cheesecake sold in Virginia, Maryland, North Carolina and Washington D.C. The product contains undeclared pecans. Consumers should stop using the product and contact Wegmans for refund or replacement.
MAYEJ COMERCIALIZADORA S. de R.L. de C.V. recalled 1,288 boxes of Italian Parsley on September 26, 2025. The recall follows concerns over contamination with Cyclospora cayetanensis, a harmful pathogen. Consumers should avoid consumption and seek refunds immediately.
Wegmans Food Markets is recalling 521 units of Large Ultimate Fresh Fruit Topped Cheesecake sold in Virginia, Maryland, North Carolina and Washington, D.C. An allergen labeling omission leaves pecans undeclared. Consumers should not eat the product and should contact Wegmans for refund or replacement.
Albertsons Companies recalled store-made Basil Pesto Bow Tie Pasta Salad sold under banners including Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons after Listeria monocytogenes contamination. The bowtie pasta ingredient used in the deli item was recalled for this reason. Consumers who purchased the product should not consume it and should contact Albertsons Companies for refund or
The recall was issued on September 26, 2025. It covers Ready Meals Smoked Mozzarella With Hot Links Extra Large sold under Carrs-Safeway, Eagle, and Safeway banners in Alaska and multiple other states. The cause is Listeria monocytogenes linked to a recalled Penne pasta ingredient used in store-made deli items. Consumers should not eat the product and should contact Albertsons Companies LLC for a