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.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Saint Francis Apizza LLC is recalling 1,920 units of Frozen Supreme Pizza due to undeclared soybean oil and soy lecithin. The product was distributed in Kentucky and Ohio.
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
Queso Palmita GP LLC is recalling 20 packages of frozen Pastel de Queso (Cheese Pie) in Texas due to undeclared milk.
Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.
Saint Francis Apizza LLC is recalling 4,255 units of frozen cheese pizza due to undeclared soy ingredients. The product was distributed in Kentucky and Ohio.
Saint Francis Apizza LLC is recalling 2,655 units of frozen Mushroom & Onion Pizza in Kentucky and Ohio due to undeclared soy ingredients.
J K Patisserie & Bakery LLC is recalling croissants because egg was not declared in the Contains statement. The product was distributed in New York and New Jersey.
J K Patisserie & Bakery LLC is recalling 87 units of Lemon Blueberry Loaf because the product contains undeclared soybean oil and soy lecithin.
Saint Francis Apizza LLC is recalling 4,931 units of frozen pepperoni pizza due to undeclared soybean oil and soy lecithin.
PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.
J K Patisserie & Bakery LLC is recalling 610 units of chocolate chip cookies sold in New York and New Jersey because soy was not declared in the Contains statement.
FreshPoint Central Florida, Inc. is recalling 1,093 units of Cranberry Chicken Salad Wedges because the egg allergen is missing from the 'Contains' statement on the label.
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.
BioSpectra, Inc. is recalling 200 kg of Tris/Tromethamine API distributed in California because the product failed stability specifications.
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries.
Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide.
G L Mezzetta Inc is recalling 32 fl oz jars of Golden Greek Peperoncini Medium Heat due to potential contamination with mice.
AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications.