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 deaths or serious injuries are reported, 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
BioPro is recalling Titanium MPJ toe implants (Lot 125651) with inaccurate labeling claiming MR compatibility when the implant has not been tested for magnetic resonance safety. Patients should consult their physician before MRI.
MEDLINE recalls Micro-Kill Bleach Germicidal Wipes due to out-of-specification low levels of sodium hypochlorite, the active disinfecting ingredient. Affected batches may have reduced effectiveness.
Acorn Stairlifts Inc. is recalling multiple stairlift models because the seats may not have adequate strength to consistently support users during continued use, creating a fall hazard.
ROi CPS LLC is recalling 50 kits of Regard TOTAL HIP implants distributed in Missouri due to incorrect product identification labeling on individual kits. This mislabeling could result in the wrong implant being used in surgery.
Beckman Coulter is recalling 181,776 AU/DxC AU Magnesium test kits because the test may give falsely elevated results in lipemic samples, potentially affecting clinical interpretation.
Abbott Molecular is recalling 3063 kits of Alinity m Integrated Reaction Units due to potential detachment of reaction vessels from the unit cap during transport. No injuries have been reported.
Microbiologics Inc is recalling KWIK-STIK quality control kits containing Enterococcus faecalis because certain lots are susceptible to Gentamicin Synergy when they should be resistant. The defect could affect laboratory testing accuracy.
Microbiologics Inc is recalling Helix Elite Molecular Standards for inactivated RSV A because real-time shelf life testing failed at 24 months, indicating the product may not maintain stability through its claimed expiration date.
Stryker is recalling MEDPOR Titan OFW implants after one unit was found with an incorrectly placed barrier layer. The defect resulted from manufacturing error rather than design.
Great Value Restaurant Style White Corn Tortilla Chips are being recalled due to potential metal contamination. Affected products have lot codes 122051## or 123051## with a best-by date of May 23, 2022.
Shimadzu recalled 28 Digital Angiography Systems with Generator Model D150GC-40 due to inadequate installation adjustment criteria that may cause x-ray radiation dose rates to exceed safe fluoroscopic imaging limits.
Intuitive Surgical is recalling the da Vinci Xi and X 12-8 mm Conductive Cannula Reducer because the metal tip may dislodge from the plastic shaft. If unnoticed, additional surgery may be needed, or energy leakage could cause tissue damage.
BioPro recalled titanium toe implants due to incorrect claims in documentation about magnetic resonance (MR) compatibility testing that was never conducted. The FDA issued a Class II recall to address the misleading safety information.
Lacrimedics is recalling approximately 5,767 units of OPAQUE Lacrimal Plugs due to potential defects in the sterile pouch seal that could compromise product sterility. The affected devices were distributed nationwide and internationally.
Shimadzu Medical Systems is recalling Digital Angiography System generators due to potential excessive x-ray radiation in fluoroscopic mode. Installation issues may cause radiation dose rates to exceed safe limits.
Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.
Kia is recalling 2022 Sorento Hybrid and Sorento PHEV vehicles because the front seatbelt pretensioner(s) may explode during a crash, potentially projecting metal fragments at occupants. Dealers will replace the pretensioners at no cost.
Hyundai is recalling 2022 Elantra and Elantra HEV vehicles because the front passenger-side seat belt pretensioner may explode during a crash, projecting metal fragments that could strike and injure vehicle occupants.
About 700 Ski-Doo snowmobiles from 2020–2022 are recalled because fuel can leak from the tank vent onto hot components when tilted or flipped, posing a fire hazard. BRP has received five reports of fires but no injuries.
Jayco and Entegra motorhomes from 2018–2023 may have defective tire valve stem extensions that contact the wheel rim, causing damage and potential tire pressure loss that increases crash risk.
Dole Fresh Vegetables is recalling Presidents Choice 12.25 oz Ranch Kits due to Listeria monocytogenes detected in harvest equipment used for raw iceberg lettuce. Affected products have codes beginning with W and best-by dates of December 22, 2021 through January 9, 2022.
Dole is recalling 10oz Very Veggie lettuce after Listeria monocytogenes was detected in harvest equipment. Affected products have best-by dates from December 23, 2021 through January 8, 2022.
Dole recalled shredded lettuce after harvest equipment tested positive for Listeria monocytogenes. Affected products with 'B' codes and best-by dates of December 23, 2021–January 8, 2022 were distributed in the US and Canada.
Dole Fresh Vegetables Inc is recalling the 9.1oz Peppercorn Ranch Chopped Kit due to potential Listeria monocytogenes contamination detected in harvest equipment. Affected products were distributed across the United States and Canada with best-by dates between December 23, 2021 and January 8, 2022.
Dole Fresh Vegetables Inc is recalling Presidents Choice Southwest Salad Kit due to potential Listeria monocytogenes contamination from harvest equipment used to collect raw iceberg lettuce for the product.