Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Gina Marie Bakery LLC recalled 172 cases of Toasted Almond & Cherry Biscotti after the FDA flagged undeclared Red 40. The recall is classified as high hazard. Consumers should avoid the product and contact the company for refunds or replacements.
Gina Marie Bakery LLC recalls 172 cases of Vanilla Chocolate Dipped Cookies after undisclosed Red 40 pigment was found. The recall was initiated by the state of Connecticut and notified to FDA on 2025-09-10. Consumers who bought the cookies should not eat them and should seek refunds or replacements.
Biomet recalled 40 Juggerknot Mini Soft Anchors, model 912080, distributed nationwide in the United States. The outer carton label lists JuggerKnot 1.0mm Mini devices, but the cartons contain JuggerKnot 1.4mm Short devices. Patients and clinicians should stop using the device and follow the recall instructions provided by Biomet.
BioPro recalled 147 femoral head components distributed in the US. The devices cover metal cobalt chromium and ceramic heads in sizes 22, 28, 32, 36 and 40 millimeters. The recall cites a packaging defect that could compromise the sterile barrier. If implanted, the loss of sterility could pose infection risk. Hospitals and surgeons should follow BioPro recall instructions immediately.
MedicalCommunications GmbH recalled 474 Ashvins HEYEX 2 / HEYEX PACS software units distributed nationwide in the United States. The affected software versions range from 2.6.0 (Build 2088) to 2.6.8 (Build 2220). The hazard is that the measured value may be smaller than the actual area, potentially affecting imaging measurements. Stop using the software immediately and follow manufacturer recall‑s
NOXBOX LTD recalled 1,667 NOxBOXi Nitric Oxide Delivery System units distributed in Tennessee after reports of flow and dose fluctuations. The device can show fluctuations when the total flow through its sensor drops below 0.5 LPM. Dose fluctuations have been observed with LifePulse HFJV or conventional ventilators under certain settings. Stop using the device immediately and follow the recall. NO
Hale Inc. recalls 54 bottles of Lotsa Pasta International Food Shop Roasted Garlic Infused Olive Oil sold in Kentucky after concerns of Clostridium botulinum contamination. The product was manufactured without an approved processing. Consumers who purchased the oil should not consume it and should contact Hale Inc for refund or replacement.
BioPro recalled 147 BioPro Femoral Head hip implant components sold in Texas and Michigan after a packaging defect could compromise sterility. The defect may result in loss of sterility, creating a risk of infection if implanted. Hospitals and clinicians should stop using the devices and await manufacturer instructions.
Hale recalled 54 bottles of Fresh Basil Infused Olive Oil sold in Kentucky after a recall notice citing potential botulism contamination. The FDA enforcement report H-0241-2026 documents the issue. Consumers should not consume this product and should contact Hale for refunds or replacements.
Drӕager recalled 530 Atlan A350 anesthesia workstations imported from Draegerwerk AG and Co. KGaA and distributed to 25 U.S. states and more than 30 countries. The device can experience a piston ventilator failure before use or fail to ventilate during use. Hospitals should stop using affected units immediately and follow Draeger recall instructions.
Draeger recalls 223 Atlan A350XL anesthesia workstations distributed in 25 states and many countries after reports of piston ventilator failure and mechanical ventilation failures. The recall affects units imported from Draegerwerk AG and Co. KGaA. Stop using the device immediately. Contact Draeger for instructions and patient safety guidance.
Whole Foods Market recalled 6-pack granola sold at one Philadelphia store after undeclared wheat, sesame and cashew were found. The product was labeled incorrectly. Consumers should not eat the product and should seek refund or replacement from WFM Purchasing, LP.
BioPro recalled 147 bipolar heads due to a potential packaging issue that may compromise sterility. The defect could result in infection if the device is implanted. Patients and healthcare providers must stop using the device immediately and follow recall instructions.
NOXBOX recalled 1,667 NOxBOXi Nitric Oxide Delivery System units sold in Tennessee. The recall was issued Sept. 9, 2025. An internal fault can occur when users press the interface rapidly without waiting for the device to respond. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.
BioPro recalled 147 Endo Head Ceramic implant components distributed in Texas and Michigan after packaging could compromise the sterile barrier. The defect could result in loss of sterility of the device, creating an infection risk if implanted. Clinicians and patients should stop using the devices and contact BioPro for instructions and refunds.
Eureka recalled 32 cases of cinnamon on September 9, 2025, due to elevated lead levels. Consumers should not consume the product and seek refunds. The recall affects retail and wholesale customers in California and Michigan.
Lee K of NY Inc. recalls 43 units of PINOCCHIO CATERING Aged Kimchi Mackerel sold in New York and New Jersey for undeclared milk and shrimp. The recall is Class I with a high hazard. Consumers should not consume the product and should contact the company for refunds or replacements.
Iantrek recalled 198 C-Rex UNO Microinterventional Goniotomy Instruments, CRX-120 models, distributed nationwide to healthcare facilities. The recall cites potential compromised integrity of the sterile packaging. Healthcare providers and patients should stop using the device immediately and follow recall instructions via the manufacturer.
Iantrek recalled 1,262 CycloPen CP-300 Cyclodialysis System units distributed nationwide to medical facilities. The recall stems from a potential compromise to sterile packaging integrity. Hospitals and clinics should stop using the device immediately and follow Iantrek’s recall instructions via email.
Sandoz Inc. recalled 263 vials of Cyclophosphamide injection distributed nationwide in the United States. The recall cites cGMP deviations due to a temperature excursion during transportation. Healthcare providers and patients should stop using the product and contact Sandoz for guidance.