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
Cipla USA is recalling 15,221 pre-filled syringes of Lanreotide Acetate 120 mg/0.5 mL due to the presence of particulate matter. The prescription injectable was distributed nationwide and patients should contact their healthcare provider.
GUSTO GROUP, INC. is recalling Shrimp Paste (Klong Kone) 'M' 16 oz jars distributed to Iowa and New Jersey due to high lead levels found in testing.
Sanders Candy Factory Inc is recalling frosted almond bulk product (lot codes 058.25 & 070.25) due to elevated aflatoxin levels. The product was distributed to one customer and has not reached consumers.
Ukrop's 6" pound cakes are recalled because the label does not disclose soy, though soy is used in the product. Consumers with soy allergies should avoid this product.
Mangalm LLC recalls Tops Mixed Fruit Jam (Batch 4F1101) because it contains carmoisine, a food color not approved for use in the US.
AZ Gems, Inc. is recalling Jumbo Raw Shrimp distributed nationwide under the Member's Mark label due to elevated chloramphenicol levels.
ASK Foods Inc is recalling Publix Rice & Pigeon Peas due to undeclared soy allergen. A total of 2,078 units were distributed to Florida. Consumers with soy allergies should not consume this product.
So Delicious Dairy Free Salted Caramel Cluster Cashewmilk is being recalled due to foreign material in the product. The recall affects units distributed nationwide in the US and Canada.
House Of Flavors is recalling 2248 Banana Pudding Ice Cream (3 GAL) because it contains undeclared soy lecithin, a potential allergen for consumers with soy allergies.
Gold Star Distribution is recalling multiple TYLENOL formulations due to insanitary conditions, including rodent exposure and activity in its distribution center. All lots within expiry are affected.
Gold Star Distribution is recalling EXCEDRIN MIGRAINE 2'S nationwide due to insanitary conditions and rodent activity in their distribution center. The recall affects all lots currently within expiry.
Gold Star Distribution Inc is recalling Personal Care Ice Gel (8oz, 12 count) distributed nationwide due to insanitary conditions and rodent exposure in its distribution center.
Liquid Dayquil (12/8oz) is being recalled by Gold Star Distribution due to insanitary conditions and rodent exposure in their distribution center. The recall affects all lots distributed nationwide.
Gold Star Distribution Inc is recalling Personal Care Vaporizing Chest Rub due to insanitary conditions including rodent exposure in their distribution center. The product was distributed nationwide.
Medicrea is recalling IB3D PL Instruments Sets because the orthopedic rotation tool handle may detach from the shaft, preventing implant rotation during surgery. The Class II recall affects 44 units distributed across nine U.S. states.
Two Philips Allura Xper FD20 X-ray systems may lack proper installation of the cooling unit drip tray, risking coolant leakage onto electrical components and potential equipment shutdown.
Philips is recalling 22 Allura Xper imaging systems because the drip tray beneath the cooling unit may not be installed or properly documented. Without it, coolant could contact electrical components and cause system shutdown.
Medline medical procedure kits containing Stryker Strykeflow 2 suction irrigators are being recalled due to a 2024 design change. Irrigation solution can travel to the handpiece and battery pack, causing leaks and vaporized saline emission resembling smoke.
Medline Industries recalls pre-operative kits containing B. Braun IV administration sets because their check valve components may become stuck in open or closed positions, potentially affecting fluid delivery.
Certain Philips Allura Xper diagnostic imaging systems may be missing a cooling unit drip tray, which could allow coolant to contact electrical components and trigger system shutdown.
A drip tray beneath the cooling unit in some Philips Allura imaging systems was not installed or not adequately documented, potentially allowing coolant to contact electrical components and cause system shutdown.
Gold Star Distribution has recalled Nyquil Cold & Flu 32-count 2-packs distributed nationwide due to insanitary conditions and rodent exposure at their distribution center.
Claritin 20-count tablets are being recalled nationwide by Gold Star Distribution Inc. due to insanitary conditions, including rodent exposure and activity, identified in their distribution center.
TESTO-100 CIII testosterone pellets are being recalled due to potential microbial contamination. The manufacturer could not ensure sterility of the product. Patients in affected regions should contact their healthcare provider.
Alvogen is recalling one bottle of Levothyroxine Sodium 150mcg tablets (lot MHA21825) that was found to contain 88mcg tablets instead. The product was distributed nationwide.