Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
Lone Star Dairy Products LLC is recalling Spray Dried Dairy Powder in 25 kg bags and 1 metric ton totes due to Salmonella identification in finished product testing.
Baxter Healthcare issued a Class I correction for the Blue Ventilator Adapter Module (Volara system accessory) due to potential oxygen desaturation and lung tissue injury risk in home care settings. Specific instructions for use are being provided.
The Philips Respironics Trilogy Evo O2 ventilator's obstruction alarm may not trigger promptly, taking up to four breaths to respond. This delay could prevent timely detection of a blocked airway in patients depending on the device for breathing support.
Mentor Texas is recalling CPX 4 breast tissue expanders due to potentially dull or blunt infusion set needles that may be difficult to insert or may break during use.
Mentor Texas, LP is recalling Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips, which may be difficult to advance and could break during use.
ReCor Medical is recalling the Paradise Ultrasound Renal Denervation System catheter (Lot M4862) because it distributed 24 nonconforming units that were not approved for human use.
Medline is recalling 14,379 surgical procedure kits containing Olympus biopsy valves that may shed rubber fragments during use, potentially creating airway obstruction.
Philips is recalling the ALLURA Xper FD20 OR Table because the wired foot switch may fail to initiate X-ray imaging or cause imaging to occur intermittently, which could delay critical diagnostic imaging during surgery.
MiniMed 530G insulin pumps may deliver too much or too little insulin when positioned above or below the injection site, potentially causing dangerously high or low blood sugar.
Burlington Medical is recalling Kilt Blockers due to potential degradation of the Xenolite 800 attenuation material over time, which may reduce the product's protective lifespan.
JFE Franchising Inc is recalling Dumpling Vegetable and Loaded Dumpling Vegetable products due to the presence of glass fragments. The products were distributed across multiple U.S. states.
TG FOODS INC is recalling Divided Sunset Multi Collagen Peptides (8 oz) because the product contains eggshell membrane collagen and wild-caught marine collagen but fails to declare EGG and the specific fish species on the label.
JFE Franchising Inc is recalling three dumpling products due to possible glass fragments. Affected products include Dumpling Party Tray (20pcs and 40pcs) Vegetable varieties and Cheetos Flamin Hot Loaded Dumpling Vegetable.
Imu-Tek Animal Health is recalling Imu-Tek Colostrum-5 120 Capsules (Lot #013, Expiration 092826) because the product is potentially under-processed. The product was distributed across 29 states.
HEYTEA USA INC is recalling Coconut Drink 1 (1L cartons) because the product contains undeclared milk. Consumers with milk allergies or sensitivities are at risk.
Appco Pharma LLC is recalling Prazosin Hydrochloride Capsules due to detection of N-nitroso-prazosin impurity above acceptable limits in multiple lots distributed nationwide.
K.C. Pharmaceuticals recalls Leader Artificial Tears and related generic brands nationwide due to inability to assure product sterility. Approximately 589,848 bottles across multiple brands and retailers are affected.
Multiple brands of artificial tears eye drops are being recalled nationwide due to lack of sterility assurance. Over 1 million bottles are affected.
Appco Pharma LLC is recalling Prazosin Hydrochloride Capsules (5mg) due to nitrosamine impurity detected above acceptable limits. The recall affects 28,157 bottles distributed nationwide.
K.C. Pharmaceuticals is recalling 74,016 bottles of sterile eye drops sold under Rugby and Walgreens brands due to lack of assurance of sterility.
Medline Industries is recalling 14,379 thoracic biopsy valve kits due to rubber fragment detachment in Olympus biopsy valves. Fragments may lodge in the airway and require medical intervention.
Intuitive Surgical is recalling 6,152 da Vinci S and Si permanent cautery hook instruments due to complaints of frayed or broken pitch cables that could cause instrument malfunction during surgery.
FDA recalls eTRAX Needle System Starter Kit 18G due to an error in sensor inspection and programming. The needle tip position may be incorrectly identified on the user interface.
Burlington Medical is recalling Wrap Aprons due to potential degradation of Xenolite 800 attenuation material over time. Approximately 5,198 units distributed worldwide are affected.
Infusion sets may contain dull or blunt needle tips that could be difficult to advance or break during insertion, creating potential complications.