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
Maple Leaf Foods Inc. recalls approximately 12,036 pounds of not-ready-to-eat smoked bacon from Canada that was imported without required reinspection. No illnesses or injuries have been reported.
Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.
About 670 Sviyatp pool drain covers sold online violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using affected pools immediately and contact Sviyatp for a refund.
BMW is recalling certain 2020-2026 S 1000 RR motorcycles because vibration may cause ignition lock failure, leading to engine stalls or electrical system failures.
K&N Engineering is recalling specific K&N and Spectre replacement fuel filters because the O-ring may disintegrate, causing leaks or clogs.
BCI Foods, Inc. is recalling approximately 4,300 pounds of canned chicken noodle soup that was imported from Canada without the required import reinspection. No illnesses or injuries have been reported.
CuddleCubs Creations Baby Highchair Teething Toy Sets are recalled due to pull-string teething toys that violate mandatory toy safety standards. The silicone strings can lodge in a child's throat, creating a risk of choking and respiratory distress.
EnHomee 9-Drawer Fabric Dressers sold on Walmart.com pose a risk of serious injury or death from tip-over and entrapment if not anchored to the wall. About 16,809 units are affected.
Oscor Inc. is recalling Abiomed REF: 0052-3025 Introducer Kits for Impella heart pump due to potential leakage from the sidearm and hub region. Manufacturing issues may cause the 14Fr and 23Fr introducer sheaths to leak under the sheath cap and along hub score lines.
Chiesi USA, Inc. is recalling Cleviprex (clevidipine) injectable emulsion due to lack of assurance of sterility. The affected product is distributed nationwide.
Abiomed, Inc. is recalling ABIOMED Intro Kit heart pump introducer sheaths due to potential leakage from under the sheath cap and along hub score lines. The manufacturing defects are not visually detectable by users.
D'Dioses Coconut Ice Pops (4 oz) may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these substances should not consume the product.
W.Y. Industries, Inc. is recalling WY Duck Sauce packets because the product may contain metal fragments. The recall affects 1,120 cases distributed to New York, New Jersey, Ohio, and Pennsylvania.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Pina Colada ice pop bars because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 dyes.
D'Dioses Fruit Pops, Inc. is recalling Ice Pop D'Dioses Limon 4 oz packages because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.
D'Dioses Fruit Pops, Inc. is recalling D'Dioses Mamey Ice Pop (1 Bar, 81.7 g) because it may contain undeclared milk, pecans, pistachios, yellow #5, and red #40.
Abiomed, Inc. is recalling ABIOMED Impella CP Introducer Kit 14 Fr units worldwide due to potential introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable.
Abiomed is recalling the Impella CP heart pump set (87,277 units worldwide) due to potential leakage from the introducer sheath that cannot be visually detected by users. The defect affects the 14Fr and 23Fr introducers included in every pump set.
D'Dioses Cookies Cream Ice Pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.
Oscor Inc. is recalling the Abiomed Impella Hemostatic Peel Away Introducer System (23F) due to manufacturing defects that may cause leakage from the sidearm, under the sheath cap, or along the hub region.
Argon Medical Devices is recalling General Biopsy Tray kits containing Lidocaine HCL Injection because the kits do not meet sterility release criteria.
ABIOMED Impella CP Introducer Kit 14Fr is being recalled due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.
Argon Medical Devices is recalling T-Lok Bone Marrow Tray kits containing Lidocaine HCL Injection USP 1% because the kits did not meet sterility release criteria.
ABIOMED Impella CP heart pump sets contain introducers that may leak from under the sheath cap and along hub score lines. These manufacturing defects are not visible during use.
Abiomed is recalling ABIOMED Introducer Kit 23 Fr due to potential sheath leakage from manufacturing defects. The leakage risk is not visually detectable and affects all current batches worldwide.