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
Signature Breads is recalling 1,893 cases of frozen parbaked French dinner rolls because they may contain metal fragments. The product was distributed in New Hampshire, Pennsylvania, and Florida.
Ocean Group Inc. is recalling 504 packages of Masago Lake Smelt Roe 6 oz. because the product contains undeclared soy and wheat.
Signature Breads is recalling frozen parbaked dinner rolls due to potential metal fragments. The product was distributed in New Hampshire, Pennsylvania, and Florida.
Madison One Acme Inc. is recalling Tong Ren Tang Shenjing Shuairuo Wan because it contains unapproved human placenta, which may transmit disease.
Signature Breads is recalling frozen parbaked baguettes because they may contain metal fragments. The recall affects 1,893 cases distributed to New Hampshire, Pennsylvania, and Florida.
Philips Medical Systems is recalling DS/US Proton Feature software due to a defect that may cause incorrect dose calculations in radiation therapy planning.
Honda is recalling 2016 Civic vehicles with 2.0L engines because missing or incorrect piston circlips may cause engine seizure, increasing the risk of a crash or fire.
Kalmar is recalling 622 Ottawa T2 trucks from 2014-2016 because an unprotected power board may cause an electrical short and fire.
Vosges, LTD is recalling 135 pounds of Uncured Bacon Ganache chocolate bars sold at Trader Joe's in four states because the product contains undeclared coconut, a known allergen.
Stoughton is recalling 2015-2016 Barrett P gooseneck trailers because the upper coupler rating is lower than the trailer's GVWR, risking separation.
Marin Pasta Works is recalling 491 pounds of pork ravioli produced without federal inspection. The products were distributed to retail locations in California.
PACCAR is recalling 2015-2016 Peterbilt 365 and 367 trucks because improperly tightened drive axle nuts may cause the driveshaft to disconnect, increasing crash risk.
BMW is recalling approximately 840,000 vehicles because the driver's frontal air bag inflator may rupture during deployment, potentially causing serious injury or death.
General Motors is recalling specific 2015-2016 Chevrolet and GMC trucks and SUVs because the brake pedal pivot nut may loosen, potentially making the brake pedal inoperative.
CE North America is recalling KUL portable fan heaters sold at Bed Bath & Beyond because they can overheat and catch fire. Four fire incidents have been reported, with no injuries.
Takata is recalling specific side air bag inflators manufactured in December 2014 because a manufacturing error could cause them to rupture and propel metal fragments into the vehicle.
Honda is recalling specific 2005-2016 Acura and Honda vehicles because the driver's airbag inflator may rupture during a crash, potentially causing serious injury or death.
Sentara Enterprises is recalling specific lots of Penicillin in D5W Homepumps because the sterility of the product cannot be guaranteed.
Sentara Enterprises is recalling 12 bags of AZACTAM (aztreonam) 2GM in NS because product sterility cannot be guaranteed. The affected lots were compounded in September 2015 and distributed in Virginia and North Carolina.
Sentara Enterprises is recalling specific lots of Dextrose-NaCl (D5-1/2NS) in Homepumps because product sterility cannot be guaranteed.
Sentara Enterprises is recalling specific lots of CUBICIN (daptomycin) in NS syringes and homepumps because the sterility of the product cannot be guaranteed.
Sentara Enterprises is recalling specific lots of ZOSYN (piperacillin/tazobactam) homepumps because product sterility cannot be guaranteed. The affected products were distributed in Virginia and North Carolina.
Sentara Enterprises is recalling specific lots of Ganciclovir in NS Homepumps because product sterility cannot be guaranteed. The affected products were distributed in Virginia and North Carolina.
Cook Medical is recalling 753 Zilver 518RX Vascular Stent delivery systems because a manufacturing defect may cause the catheter joint to separate during use.
Sentara Enterprises is recalling Meropenem in NS Homepumps because product sterility cannot be guaranteed. The recall affects 192 bags distributed in Virginia and North Carolina.