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.
Ferrara is recalling 2013-2014 Igniter and Inferno firetrucks because loose front suspension ball joints may separate, causing loss of steering control and increasing crash risk.
Fontaine Trailer Company is recalling 2015 Traverse HT trailers because a suspension member may separate from the trailer, increasing the risk of a crash.
Honda is recalling 2015 Fit vehicles because damaged ignition coil wires may cause the engine to stall, increasing crash risk.
General Motors is recalling 2013-2016 Cadillac ATS sedans because the rear defogger system may overheat, increasing the risk of a fire.
Kenosha Beef International is recalling approximately 89,235 pounds of Johnsonville pork sausage patties that may contain small pieces of metal.
Liberty Drug & Surgical is recalling 2 vials of Papaverine/Phentolamine/PGE-1 Injectable because process deficiencies may have compromised sterility.
Reckitt Benckiser is recalling Mucinex Fast-Max Cold & Sinus liquid because the back of the bottle is missing active ingredients and safety warnings.
Fresh Unlimited Inc is recalling Kale Chicken Caesar Pasta Salad because the product labels failed to declare the allergen eggs.
Fresh Unlimited Inc. is recalling Kale Caesar Pasta Recovery Salad because the product labels failed to declare the allergen eggs.
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling 22 vials of Dexamethasone 24 mg/mL Injectable due to process deficiencies that could have compromised sterility.
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling 85 vials of 17-Hydroxyprogesterone injectable because process deficiencies may have compromised sterility.
Liberty Drug & Surgical is recalling Lidocaine/Sodium Chloride injectable vials because process deficiencies may have compromised sterility.
Reckitt Benckiser is recalling Mucinex Fast Max Night Time Cold & Flu liquid bottles because the back label is missing active ingredients and safety warnings.
Liberty Drug & Surgical is recalling Papervine/Phentolamine/PGE-1 Injectable vials because process deficiencies may have compromised sterility.
Liberty Drug & Surgical is recalling Papaverine/Phentolamine/PGE-1 Injectable vials because process deficiencies could have compromised the product's sterility.
Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles where the back label is missing active ingredients and safety warnings.
The Kroger Co is recalling specific containers of Kroger Garlic Powder because a sample tested positive for Salmonella. The recall covers items produced on the filling line between sanitation cycles.
Liberty Drug & Surgical is recalling Glycerin 72% Injection vials because process deficiencies may have compromised sterility. The product was distributed to physicians and facilities in NJ and NY.
GlaxoSmithKline is recalling Bactroban Cream (mupirocin calcium) 2% because the product was contaminated with penicillin and foreign substances during manufacturing.
Liberty Drug & Surgical is recalling Papaverine/Phentolamine/PGE-1 Injectable vials because process deficiencies may have compromised sterility.
Barrel O' Fun Snack Foods is recalling one lot of Vic's Original White Popcorn because it contains an undeclared milk allergen.
Fresh Unlimited Inc is recalling Caesar Salad kits because the labels failed to declare the presence of eggs, a major food allergen.
Liberty Drug & Surgical is recalling 58 bags of Doxycycline IV solution because process deficiencies may have compromised sterility.