Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. 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.
Halcore is recalling 55 AEV ambulances because a suspension fluid tank bracket may fail, causing the tank to separate and create a road hazard.
Honda is recalling 2015 Acura TLX vehicles because a transmission defect may prevent the vehicle from engaging Park, increasing the risk of rolling away and crashing.
Pierce Manufacturing is recalling 2008-2011 Quantum fire apparatus because broken accelerator pedal springs may cause unintended acceleration, increasing crash risk.
Ford is recalling 2014 Transit Connect cargo vans because sliding door panels may separate while driving, increasing crash risk.
Horizon Hobby is recalling HobbyZone Super Cub S power supplies and chargers because they can overcharge batteries, posing a fire and property damage risk.
Quality Meats, Inc. is recalling approximately 44,372 pounds of frozen pork belly because the product was not presented for USDA-FSIS import inspection.
Toshiba American Medical Systems is recalling two units of cardiac function analysis software because it may display incorrect analysis results for heart function.
nSpired Natural Foods is recalling MaraNatha Organic Raw Creamy Almond Butter due to potential Salmonella contamination. The product was distributed in the US, Canada, and other countries.
Perry Drug Inc. is recalling Cyclosporine 0.045% eye drops due to potential sterility assurance issues identified during an FDA inspection.
nSpired Natural Foods is recalling specific lots of MaraNatha and Whole Foods 365 almond butter due to potential Salmonella contamination.
Perry Drug Inc. is recalling HCG 200 IU/mL Injection vials in Kansas and Missouri due to potential sterility assurance issues identified during an FDA inspection.
Perry Drug Inc. is recalling 20 vials of compounded Sodium Tetradecyl Sulfate 0.3% Injection in Kansas and Missouri due to potential sterility assurance issues found during an FDA inspection.
nSpired Natural Foods is recalling MaraNatha No Stir Crunchy Almond Butter due to potential Salmonella contamination. The product was distributed in the US, Canada, and other countries.
Kerry Foods is recalling 148 bags of Breakfast Sausage Seasoning because an ingredient tested positive for Salmonella.
Kerry Foods is recalling specific lots of Sausage Crumble because an ingredient tested positive for Salmonella.
Perry Drug Inc. is recalling 17 vials of compounded Tri-Mix in Kansas and Missouri due to quality control issues affecting sterility assurance.
Hospira is recalling 305,664 bags of Normosol-R Multiple Electrolytes Injection due to potential punctures that may compromise sterility and cause leaks.
Karlsburger Foods is recalling Low Sodium Taco Seasoning because it contains milk, an allergen not declared on the label.
Baxter Healthcare is recalling Heparin Sodium in Sodium Chloride Injection because the raw material was found to have low potency.
Perry Drug Inc. is recalling specific lots of compounded Phenylephrine HCl syringes due to quality control issues affecting sterility assurance.
Perry Drug Inc. is recalling HCG injections due to quality control issues that may compromise sterility assurance.
nSpired Natural Foods is recalling MaraNatha No Stir Crunchy Peanut Butter due to potential Salmonella contamination. The product was distributed in the US, Canada, and other countries.
Hospira is recalling 153,504 bags of Sterile Water for Injection due to potential punctures that may compromise sterility and cause leaks.
Perry Drug Inc. is recalling Tri-mix Antidote syringes in Kansas and Missouri due to potential sterility assurance issues identified during an FDA inspection.
Perry Drug Inc. is recalling Tri Mix PF SYR 0.5 mL Inj. syringes in Kansas and Missouri due to potential sterility assurance risks identified during an FDA inspection.