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.
Eddy Packing Co. is recalling approximately 49,558 pounds of smoked sausage products due to possible contamination with hard plastic. No illnesses or injuries have been reported.
Forest River is recalling 2018 Surveyor recreational trailers because a missing fan in the slide-out refrigerator may cause overheating and increase the risk of a fire.
General Motors is recalling 2014-2017 Chevrolet Express and GMC Savana vans because liquid leakage in the driver's window switch can cause corrosion and increase the risk of a fire.
Porsche is recalling 2015 918 Spyder vehicles because rear suspension connecting shafts may fail due to stress corrosion cracking, increasing the risk of a crash.
Navistar is recalling 2018-2019 International trucks and buses because the front seat belt anchor bolt may break in a crash, increasing injury risk.
Jayco is recalling 2018 Eagle HT fifth wheel trailers because a spindle placement error in the pin box may cause the bearing to become loose, increasing the risk of a crash.
Navistar is recalling 2019 IC Bus CE school buses because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.
Navistar is recalling 2017-2019 International HX trucks because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.
Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vans because missing spot welds may reduce body strength in a crash.
Coastal Meds, LLC. is recalling 1,506 vials of Hydroxocobalamin Injectable due to the presence of unknown particulate matter. The product was distributed nationwide.
Seabear Company is recalling 2,080 units of Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeled storage instructions.
Premier Pharmacy Labs is recalling specific lots of Morphine Sulfate Injection because routine testing of other lots detected microbial contamination risks.
Coastal Meds, LLC. is recalling 635 vials of Pyridoxine Injectable due to the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling LIPO-PLEX Injectable-30 mL vials nationwide due to the presence of unknown particulate matter.
Premier Pharmacy Labs Inc is recalling 4,192 syringes of Morphine Sulfate 4 mg/mL PF Injection due to a lack of assurance of sterility.
Becton Dickinson is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Kitchen by the Sea is recalling Bloody Mary mix because the labels failed to list egg, soy, wheat, and sulfites.
Thor Motor Coach is recalling 2011-2017 Tuscany and Venetian motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.
Seabear Company is recalling 381 units of Hot Smoked Keta Beergarden Salmon due to water phase salt deviations and mislabeled storage instructions.
Premier Pharmacy Labs is recalling 3,570 hydromorphone syringes because routine testing of other lots found microbial contamination risks.
Volkswagen is recalling 2018 Atlas vehicles because a manufacturing error may cause the fuel tank to leak, increasing the risk of a fire.
Coastal Meds, LLC. is recalling 3,733 vials of LIPO-DEN EXTREME Injectable-30 mL due to the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling 200 vials of ADENO-PLEX Injectable-30 mL MDV due to the presence of unknown particulate matter.
Ion Beam Applications is recalling five Proteus proton beam therapy systems because a software error may cause under-irradiation or additional X-ray exposure.
Premier Pharmacy Labs is recalling NeoStigmine Methylsulfate syringes because routine testing of other lots detected microbial contamination risks.