Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Taproom Gourmet bulk Empire Mix recall affects 3,547 cases distributed across New York, New Jersey, Connecticut, California, Illinois and Florida. The product lacks an ingredient label and contains undeclared allergens. Consumers should not consume the product and should seek a refund or replacement from Egress Capital Partners.
Kirkland Signature Ahi Tuna Wasabi Poke sold at Costco is recalled after a Listeria monocytogenes positive test in green onions used in the product. Western United Fish Company initiated the recall. Consumers should not eat the product and should seek refunds or replacements.
GE Medical Systems recalled 31 LOGIQ P10 R4.5 HD ultrasound systems sold nationwide in the United States and globally after discovering UGAP measurements may misstate liver steatosis. The UGAP data may display inaccurate values representing liver steatosis. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.
Garden Fresh Foods Inc. recalled 540 pounds of sliced green onions on September 18, 2025. The product may be contaminated with Listeria monocytogenes. This recall affects only Washington state.
Cardinal Health 200, LLC recalled Salem Sump gastroduodenal tubes worldwide after reports of anti-reflux valve breakage. The ARV can fail under excessive force during use. Healthcare providers and patients should stop using the device immediately and follow the manufacturer instructions for recall communication.
Glenmark Pharmaceuticals Inc. USA recalls 13,824 tubes of azelaic acid gel 15% after CGMP deviations prompted gritty texture complaints. The recall covers nationwide distribution in the United States. Consumers should stop using the product and contact Glenmark for guidance.
Haifa Cold Smoked Sea Bass 8 oz distributed by D & M Smoked Fish is recalled after 348 pieces were found contaminated with Listeria monocytogenes. The recall was issued Sept. 17, 2025, with FDA update on Oct. 22, 2025. Consumers should not eat the product and should contact D & M Smoked Fish for refunds or replacements.
Baxter Healthcare recalled 5,209 oral/axillary probes used with Welch Allyn SureTemp Plus thermometers nationwide in the United States, Canada and Colombia. The probes were inadvertently programmed with the rectal configuration, which can yield a lower temperature reading. Healthcare providers and patients should stop using the affected probes immediately and follow Baxter’s recall instructions.
D & M Smoked Fish, Inc. recalls 2,022 Haifa Cold Smoked Salmon, 8 oz packages distributed in NY, NJ, PA, WA, CA, IL and FL after Listeria monocytogenes was detected. The recall is classified as high risk. Consumers who bought this product should not eat it and should contact D & M Smoked Fish for a refund or replacement.
CPM Medical Consultants recalls 3,317 Fuse ULTRA Foot Plating System Instructions for Use issued nationwide in the United States. The recall addresses sterilization steps that are no longer required in the United States. Healthcare providers should stop using the current IFU and follow CPM’s recall instructions.
Enterix recalled 201,426 InSure ONE Fecal Immunochemical Test kits after a sensitivity failure linked to Test Card Lot TT241102. The issue may cause false negative results. Healthcare providers and patients should stop using the affected kits and follow the manufacturer’s recall instructions.
PepsiCo's Lipton Green Tea Citrus RTD bottles, sold at multiple retailers, are recalled after undeclared sugar was found in the finished product. A labeling error shows 25g sugar on the outer case while individual bottle labels show 0g. Consumers should not drink this product and should contact PepsiCo for refunds or replacements.
Percussionaire recalled 59,160 Phasitron 5 IPV In-Line Valve sets worldwide after an IFU update flagged a pressure-relief leak when used with ventilators. The defect endangers neonates and infants and patients under 10 kg with tidal volumes under 50 mL. Healthcare providers should halt use immediately.
Park Avenue Compounding recalled 858 syringes of Phenylephrine HCI on September 17, 2025, due to CGMP deviations. The recall affects syringes with Lot # 20250813-13D65E and an expiration date of February 9, 2026. Consumers must stop using the product immediately and consult healthcare providers for further guidance.
IntegraDose Compounding Services recalled 853 IV bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride. The recall is nationwide in the United States. Testing found no oxytocin in the IV bags. Stop using the product and contact IntegraDose or a healthcare provider for guidance.
Abiomed recalled 9,177 distributed Automated Impella Controllers worldwide over purge pressure concerns linked to purge retainer failures. The recall covers multiple product codes, including AIC w/Impella Connect for ECP (1000432) and various packaged controllers. Hospitals and clinicians should stop using the device and follow the manufacturer's recall instructions immediately.
Accord Healthcare recalled 54,432 bottles of Levothyroxine Sodium Tablets, USP, 88 mcg, distributed nationwide in the United States. The recall is due to subpotent assay content observed during long-term stability testing. Patients should stop using the product immediately and contact Accord Healthcare or their healthcare provider for guidance.
Sprout Organics recalled 9,873 cases of 6+ Months Made With Organic Sweet Potato, Apple & Spinach baby food nationwide. A potential contamination with lead has been identified. Consumers who purchased the product should stop using it and contact Sprout Organics for refund or replacement through the recall notice.
Lawrence Wholesale recalled 4,871 cases of frozen tail-on shrimp sold through Kroger stores in 16 states. The products were manufactured under insanitary conditions and may be contaminated with Cesium-137. Consumers should not eat these shrimp and should contact Lawrence Wholesale LLC for refunds or replacements.
Lawrence Wholesale recalled 8,400 cases of Shrimp Cocktail Bowl products sold to Kroger stores in 15 states on Sept. 16, 2025 due to potential Cesium-137 contamination. The recall involves 7oz and 17oz clear plastic bowls with UPCs 011110622952 and 011110624840. Consumers should not consume the product and should contact Lawrence Wholesale LLC for refund or replacement by email.