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
Royal International Trading Inc. is recalling Tainy Boctoka Dry Fruits Mix because the product contains undeclared sulfites.
Philips Ultrasound Inc is recalling S8-3t transesophageal transducers that may fail to measure tip temperature correctly, potentially preventing auto-cooling and causing patient injury.
ICU Medical is recalling 675 IV administration sets that may contain a 15 drops/mL cannula instead of a 10 drops/mL cannula, risking under-delivery of critical medication.
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Argon Medical Devices is recalling specific 0.035-inch guidewires because the soft tip stiffness caused tissue perforation. The affected units were distributed to several countries outside the US.
ICU Medical is recalling 50 units of 10 Drop Primary IV Sets because they may contain 15 drops/mL cannulas, risking under-delivery of critical medications.
LiquidSpring is recalling specific suspension systems for 2019-2020 RAM 4500 and 5500 vehicles because the rear brake line may wear, causing brake failure.
Applied Medical Resources Corp is recalling 28,799 Dual Lumen Graft Cleaning Catheters due to reports of tip separation during use, which may expose patients to unintended dislodgement.
ICU Medical is recalling veterinary IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of medication.
ICU Medical is recalling IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of critical medication.
ICU Medical is recalling 14,000 IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of critical medication.
Volkswagen Group of America is recalling 2020 Audi A6, A7, and Allroad vehicles because the passenger airbag may not deploy properly, increasing injury risk.
Maquet Cardiovascular is recalling specific Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Porsche is recalling 2,253 Cayenne vehicles because a fuel line connector may leak, increasing the risk of fire.
Ideal Foods is recalling approximately 3,302 pounds of meat and poultry flatbread pizzas produced without federal inspection. No adverse reactions have been reported.
Ford is recalling 2014-2017 Transit Connect vehicles with panoramic roofs due to a bonding defect that could cause the roof to separate while driving.
Blue Bird is recalling 2020-2021 Vision and All American school buses because the foot pedal parking brake assembly may be improperly assembled, potentially failing to hold the vehicle on an incline.
Maintainer is recalling 16 modified 2019-2020 International CV and Chevrolet Silverado tow vehicles because incorrectly installed Power Take Offs may loosen, risking transmission fluid loss and rear wheel lockup.
Blue Bird is recalling 2020-2021 Vision and 2021 All American buses because the parking brake may fail to hold the vehicle on an incline.
Navistar is recalling 2018-2020 International LT and 2019-2020 RH trucks because a wrist pin bushing failure may cause unexpected engine shutdown and increase crash risk.
General Motors is recalling 2,281 vehicles due to potential loss of electric power steering assist caused by connector corrosion.
Whole Foods Market is recalling Minestrone Soup sold in deli containers and bags because it may contain undeclared milk.
Philips North America is recalling 346 TraumaDiagnost X-Ray systems because a shaft may break due to material fatigue, causing the arm to fall and potentially injure patients or staff.
Amneal Pharmaceuticals is recalling Nizatidine Oral Solution because it may contain N-Nitrosodimethylamine (NDMA) levels above FDA limits.
Freedman Food Service is recalling frozen flounder stuffed with seafood due to undeclared wheat, soy, eggs, and milk.