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
Aston Martin is recalling 2011-2014 V8 Vantage vehicles because a broken clutch fluid line connector may cause hydraulic leaks, preventing gear shifting or causing the vehicle to roll away.
Bausch & Lomb is recalling specific lots of NasalCrom nasal spray due to potential microbial contamination in the manufacturing water.
GE Healthcare is recalling Infant Warmer Systems because loose screws in the heater head could fall and cause thermal injuries to patients.
Channel Fish Processing Co., Inc. is recalling approximately 1,190 pounds of breaded Swai products because they may contain undeclared milk, a known allergen.
Cummins is recalling X15 heavy-duty diesel engines because a fuel pump drive gear may slip, causing engine stalls and increasing crash risk.
Embutidos Fanguito, Inc. is recalling pork products due to mislabeling, misbranding, and undeclared allergens. The products were distributed to retail locations in Florida.
KTM is recalling 2016-2017 690 Duke motorcycles because the fuel tank filler cap area may leak, increasing the risk of fire or injury.
Entegra is recalling 2012-2015 Cornerstone motorhomes because a starter motor component may break, causing overheating and increasing the risk of a fire.
Triple E RV is recalling 2016-2017 Wonder motorhomes because missing frame bolts may cause structural distortion and affect vehicle control.
Supreme Cuisine is recalling approximately 325,000 pounds of meat and poultry fat and lard products due to a processing deviation that may allow bacterial pathogens to grow.
Channel Fish Processing Co. is recalling approximately 840 pounds of breaded Swai fillets because they may contain undeclared milk, a known allergen.
Embutidos Fanguito, Inc. is recalling approximately 454 pounds of sliced pork ham products due to mislabeling, misbranding, and undeclared allergens.
Thor Motor Coach is recalling 2018 Outlaw 29H motorhomes because an incorrect fuse size may increase the risk of a fire if the awning light circuit short circuits.
Hilo Fish Company is recalling Krimson Brand Tuna Steaks after independent lab testing found positive results for Hepatitis A.
Golden Platter Foods Inc. is recalling approximately 31,662 pounds of ready-to-eat poultry and beef products due to misbranding and undeclared milk, a known allergen.
Hilo Fish Company Inc. is recalling 199 cases of frozen yellowfin tuna cubes after independent lab testing found positive results for Hepatitis A.
Arrow International is recalling VPS Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Lamb Weston is recalling Red Robin Crispy Onion Rings because the frozen product contains undeclared milk, a major food allergen.
Magellan Diagnostics is recalling LeadCare and LeadCare II test kits because they may underestimate lead concentrations in venous blood samples.
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets because connection issues may cause leaks and contamination, potentially leading to peritonitis.
Arrow International is recalling MAC Two-Lumen Central Venous Access Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Arrow International is recalling Arterial Catheterization Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Newmar is recalling 2012-2015 King Aire and Essex motorhomes because a starter motor component may break, causing overheating and increasing the risk of a fire.
Laserex Systems Inc. is recalling 83 Ellex Tango Reflex laser ophthalmic units because they may emit laser energy without the fire button being pressed.
Arrow International is recalling 43,394 units of ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kits nationwide due to safety cover disengagement and needlestick injury risks associated with packaged BD Eclipse Needles.