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
Fresenius Kabi is recalling specific batches of 0.9% Sodium Chloride Injection because sterility cannot be assured. The affected batches were distributed nationwide, including Alaska and Puerto Rico.
Fresenius Kabi recalls 0.9% Sodium Chloride Injection due to lack of sterility assurance. Multiple batches distributed nationwide are affected; patients should contact their healthcare provider.
GE Healthcare is recalling OMNIPAQUE (iohexol) injection vials nationwide due to presence of particulate matter. The affected lots are distributed throughout the U.S.
Cipla USA recalls Lanreotide Acetate Injection nationwide due to manufacturing deficiencies in visual inspection procedures affecting sterile assurance. No illnesses have been reported.
Fresenius Kabi is recalling 5% Dextrose Injection due to lack of assurance of sterility. The affected batch was distributed nationwide in the US, including Alaska and Puerto Rico.
Teva Pharmaceuticals is recalling Clonidine Transdermal System patches (0.3 mg/day) due to use of an unapproved raw material in manufacturing. Approximately 113,943 cartons were distributed in the United States.
Fresenius Kabi USA is recalling batch 6402165 of 5% Dextrose Injection (NDC 65219-458-05/30) due to lack of assurance of sterility. The batch was distributed nationwide through May 30, 2028 and should not be used.
Fresenius Kabi is recalling specific batches of 5% Dextrose Injection due to lack of assurance of sterility. The affected batches were distributed nationwide, including Alaska and Puerto Rico.
Fresenius Kabi USA, LLC is recalling multiple batches of 0.9% sodium chloride intravenous injection due to lack of sterility assurance. No illnesses have been reported, but non-sterile IV solutions pose a risk of serious infection.
Artificial Tears glycerin eye drops made by Preferred Pharmaceuticals are being recalled due to lack of sterility assurance. The 0.5 oz bottles were distributed nationwide.
Fresenius Kabi recalled specific batches of 0.9% Sodium Chloride Injection due to lack of sterility assurance. Affected batches were distributed nationwide, Alaska, and Puerto Rico.
Fresenius Kabi USA is recalling specific batches of 0.9% sodium chloride injection due to lack of assurance of sterility. The product is distributed nationwide, Alaska, and Puerto Rico.
Teva Pharmaceuticals is recalling Isotretinoin 40 mg capsules in specific lots due to potency variation issues, affecting 8,376 packages distributed to FL, OH, PR, and MS.
Fresenius Kabi USA, LLC is recalling specific batches of 0.9% Sodium Chloride Injection due to lack of assurance of sterility. Patients who have this product should contact their healthcare provider.
GE Healthcare is recalling OMNIPAQUE (iohexol) radiographic contrast injection nationwide due to the presence of particulate matter in certain lots. The recall affects 866,570 vials.
Cipla USA is recalling 54,583 units of Lanreotide Acetate injection (120 mg/0.5 mL) nationwide. The FDA identified deficiencies in visual inspection procedures at the contract manufacturing site that could compromise sterility assurance.
XTANT Medical is recalling 2 units of Xpress Pedicle Screw System from one lot mislabeled with an incorrect part number that identifies them as shorter than their actual physical length.
Cook Incorporated is recalling Arterial Pressure Monitoring Trays because the devices are labeled with expiration dates beyond their actual shelf life, creating a risk if used past their true expiration.
Cook Medical recalls drainage catheters with mislabeled expiration dates that exceed actual shelf life. Affected units may degrade before the labeled expiration date.
Riverence Smoked Trout Dip is recalled because the label does not declare milk, despite containing cream cheese. The product was distributed to California, Massachusetts, New Jersey, New York, Oregon, Texas, Utah, and Vermont.
Cook Incorporated is recalling the Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set because the labeled expiration dates exceed the devices' true shelf life. The recall affects 476 units distributed worldwide.
Cook Medical's Wayne Pneumothorax Set has incorrect labeling on 104 units. Products are labeled with expiration dates that exceed their true shelf life.
Toyota is recalling approximately 55,405 Camry and Corolla Cross Hybrid vehicles due to a loose inverter bolt that may cause loss of power or fire risk.
General Motors is recalling 2025-2026 Chevrolet Equinox EV vehicles equipped with Continental 21-inch tires that may experience tread detachment, increasing crash risk. Dealers will replace affected tires at no cost.
BISSELL is recalling about 1.7 million Steam Shot steam cleaners because attachments can unexpectedly detach and expel hot water or steam, causing burns. 206 incidents have been reported, including 161 burn injuries.