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
Family Pharmacy of Statesville is recalling Hydromorphone HCl 5 mg/mL Infusion in 250 mL bags because the manufacturer cannot assure the product meets sterility requirements.
Family Pharmacy of Statesville is recalling Morphine Sulfate 6 mg/mL infusions in 250 mL bags due to lack of assurance of sterility. The affected product was distributed in North Carolina.
Family Pharmacy of Statesville is recalling three bags of Ketamine 50 mg Infusion Solution because the manufacturer cannot assure sterility of the product.
Family Pharmacy of Statesville is recalling Methylcobalamin 1 mg/mL Injectable in 1 mL syringes (Lot #07282020@3) distributed in North Carolina because the manufacturer cannot assure the product meets sterility standards.
Albanese Confectionery is recalling specific lots of its Dark Chocolate Espresso Bean tubs due to undeclared peanut allergen. Consumers with peanut allergies who purchased this product should not consume it.
SD Biosensor's STANDARD Q COVID-19 Ag Home Test kits were illegally imported without FDA approval, clearance, or authorization. Approximately 400,000 units were distributed nationwide.
Ice cream products manufactured by Royal Ice Cream Company in Manchester, CT are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed across multiple states under various retail and food service brand names.
Mercedes-Benz is recalling specific 2007-2014 models because incorrect software updates may cause loss of drive power or control functions, increasing crash risk.
HD Premier is recalling DigitDots 3mm and 5mm magnetic balls because swallowed magnets can lodge in the digestive system, causing perforation, blockage, infection, and potentially death. Four children have required surgery to remove ingested DigitDots.
FXswede AB is recalling about 5,000 ToolGuards Portable Water Immersion Heaters sold on Amazon.com because the units can overheat, melt, or catch fire, creating electrocution and fire hazards. The firm has received 19 reports of overheating or fires and 2 reports of consumer shock.
Newmar is recalling 1,277 of its 2021 and 2022 motorhomes because the steering column bolt may not be properly tightened, potentially causing loss of steering control. Owners should contact dealers for free inspection and tightening.
Abbott Similac Pro-Total Comfort Infant Formula is being recalled due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints have been linked to these dangerous pathogens in affected infants.
Abbott Similac For Spit Up Infant Formula with Iron is recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport, with evidence of Cronobacter sakazakii found in the manufacturing facility.
Abbott recalls Similac Advance Step-1 infant formula due to Cronobacter sakazakii and Salmonella Newport detected in the product and manufacturing facility, following consumer complaints in infants.
Abbott is recalling Similac Alimentum infant formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport contamination, with evidence of Cronobacter in the manufacturing facility. The recall affects 40,943 cases.
Abbott Laboratories is recalling 22,074 cases of Similac for Supplementation infant formula due to potential Cronobacter sakazakii and Salmonella Newport contamination identified through consumer complaints and manufacturing facility testing.
Abbott is recalling Similac Sensitive Infant Formula with Iron due to potential Cronobacter sakazakii and Salmonella Newport contamination linked to consumer complaints about infant illness. The FDA classified this as a Class I recall.
Abbott is recalling Similac infant formula products for possible contamination with Cronobacter sakazakii and Salmonella Newport following consumer complaints of illness in infants.
Abbott is recalling EleCare Jr infant nutrition powder (203,416 cases) due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants and contamination found in the manufacturing facility.
Abbott is recalling Similac For Spit Up Infant Formula due to contamination risks. Consumer complaints linked the product to Cronobacter sakazakii and Salmonella Newport, and Cronobacter was found in the manufacturing facility.
Abbott is recalling EleCare Junior Vanilla infant formula due to possible contamination with Cronobacter sakazakii or Salmonella Newport. The company found evidence of Cronobacter in the manufacturing facility and received consumer complaints.
Abbott Similac PM 60/40 Low Iron Infant Formula has been recalled due to contamination with Cronobacter sakazakii and Salmonella Newport. The recall affects 8,358 cases distributed nationally and worldwide.
Abbott Similac Organic infant formula products are recalled by the FDA due to potential Cronobacter sakazakii or Salmonella Newport contamination. Consumer complaints of illness in infants and manufacturing facility contamination triggered this Class I recall.
Abbott Similac Alimentum Toddler Drink is recalled for consumer complaints related to Cronobacter sakazakii or Salmonella Newport contamination in infants, with Cronobacter sakazakii evidence found in the manufacturing facility.
Abbott Similac Pro-Sensitive Infant Formula is being recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with evidence of Cronobacter found in the manufacturing facility.