Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
KZRV is recalling 2022 Stratus, Connect, Sonic, and SportTrek travel trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.
Custom Wheel House LLC is recalling specific Method Race Wheels because the spokes may crack under heavy loads, potentially causing a loss of vehicle control.
Abbott Laboratories is recalling EleCare and Similac EleCare infant formula due to consumer complaints of Cronobacter sakazakii and Salmonella Newport infections in infants, and Cronobacter contamination in the manufacturing facility.
Lusys Laboratories' Luscient Diagnostics COVID-19 Antigen Test Kits are being recalled because they lack FDA authorization. The kits were not approved, cleared, or authorized for distribution in the United States.
Lusys Laboratories is recalling 33,955 COVID-19 antibody test kits distributed across the US and internationally because the product lacks FDA authorization, clearance, or approval for marketing or use.
Concord Farms is recalling Fresh Enoki Mushrooms due to Listeria monocytogenes contamination found by the California Department of Public Health. The affected product was distributed in California and Nevada.
American Health Packaging is recalling one lot of Oxycodone Hydrochloride Oral Solution due to impurity failure detected at initial testing of the repackaged product.
Abbott Similac Pro-Advance Infant Formula is being recalled due to potential Cronobacter sakazakii and Salmonella Newport contamination. The FDA Class I recall affects approximately 1.7 million cases distributed nationwide and worldwide.
Abbott Laboratories is recalling Similac For Spit Up Infant Formula nationwide and worldwide due to potential contamination with Cronobacter sakazakii and Salmonella Newport. The pathogens were identified through consumer complaints and detected in the manufacturing facility.
ev3 Inc. is recalling the Medtronic TurboHawk Plus Directional Atherectomy System due to design similarities to a device with reported tip detachment and embolization incidents. The FDA has classified this as a Class I recall.
Abbott is recalling multiple Similac infant formula products due to potential contamination with Cronobacter sakazakii and Salmonella Newport. These pathogens pose serious health risks to infants.
Abbott Laboratories is recalling Similac 360 Total Care Sensitive Infant Formula due to potential Cronobacter sakazakii or Salmonella Newport contamination. The recall affects products distributed in the United States and worldwide.
Abbott EleCare Jr Amino Acid-Based Nutrition Powder (banana) is recalled due to consumer complaints of Cronobacter sakazakii or Salmonella Newport in infants, with pathogen evidence in the manufacturing facility.
Abbott Similac Total Comfort infant formula is recalled due to potential contamination with Cronobacter sakazakii and Salmonella Newport, following consumer complaints in infants and evidence of the pathogen in the manufacturing facility.
Abbott is recalling Similac infant formula due to possible contamination with Cronobacter sakazakii and Salmonella Newport. The recall covers approximately 103,025 cases distributed nationwide and worldwide.
Abbott is recalling Similac Sensitive infant formula due to potential contamination with Cronobacter sakazakii or Salmonella Newport. Consumer complaints related to these pathogens in infants and evidence of Cronobacter in the facility prompted the Class I recall.
Abbott is recalling Similac Pro-Advance infant formula due to potential contamination with Cronobacter sakazakii and Salmonella Newport. Consumer complaints related to these pathogens in infants have been reported, and the bacteria was found in the manufacturing facility.
Abbott Laboratories is recalling Alimentum infant formula due to Cronobacter sakazakii detected in the manufacturing facility and consumer complaints of Cronobacter and Salmonella Newport in infants.
Abbott Similac Total Comfort Infant Formula with Iron is being recalled due to consumer complaints related to Cronobacter sakazakii and Salmonella Newport. The FDA classified this Class I recall affecting over 1.2 million cases.
Jan Fruits, Inc. is recalling Taiwan Best Quality Enoki Natural Mushrooms due to Listeria monocytogenes contamination found by California Department of Public Health. Approximately 617 cases were distributed in California.
Abbott Laboratories is recalling Similac Alimentum infant formula due to contamination with Cronobacter sakazakii and Salmonella Newport. The recall involves 34,704 cases distributed nationwide and worldwide following consumer complaints and manufacturing facility testing.
Abbott Similac Sensitive infant formula is being recalled due to consumer complaints of Cronobacter sakazakii and Salmonella Newport in infants, with evidence of bacterial contamination in the manufacturing facility.
Abbott Similac Organic with A2 Milk Infant Formula is being recalled following consumer complaints related to Cronobacter sakazakii and Salmonella Newport in infants, plus evidence of Cronobacter in the manufacturing facility.
Abbott Laboratories is recalling Batch 26811Z200 of Abbott EleCare Infant Formula Unflavoured due to consumer complaints involving Cronobacter sakazakii and Salmonella Newport in infants.
Abbott is recalling approximately 95,077 cases of Similac EleCare infant formula due to consumer complaints involving Cronobacter sakazakii and Salmonella Newport in infants, and detection of Cronobacter sakazakii in the manufacturing facility.