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.
PL Custom is recalling 2020-2024 Type 1 and Type 3 ambulances because a firmware defect may cause electrical circuits to overheat and catch fire.
E-One is recalling 408 fire trucks because a wiring defect may cause electrical circuits to overheat and start a fire.
Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.
Salm Partners, LLC is recalling ready-to-eat turkey kielbasa products due to possible contamination with bone fragments.
Braun Northwest is recalling 2020-2021 Northstar ambulances because a firmware defect may cause electrical circuits to overheat and increase the risk of fire.
Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.
Spektrum Brakes is recalling Dynamic Friction R1 brake rotors because the hub can fracture, causing a loss of braking ability and increasing crash risk.
Medline is recalling 620,735 tracheostomy care kits because the brush component has a sharp edge that can puncture tubing and injure users, and bristles can detach during use.
Magnum XXL 9800 capsules contain undeclared sildenafil and were marketed without FDA approval. The product was distributed nationwide via Amazon.
Brut Classic Antiperspirant & Deodorant in 4 oz and 6 oz aerosol cans is being recalled due to benzene contamination. The recall affects all lots distributed in the United States and Canada.
Sure Unscented Deodorant Aerosol is being recalled nationwide due to benzene contamination. Consumers should stop using affected cans and contact the manufacturer.
Medline Industries recalls 550 educational nurse training kits due to sharp edges on tracheostomy brush components that can puncture tubing or cause injury, and bristles that may detach during or before use.
Medline is recalling 172 Nursing Skills kits due to defects in the tracheostomy brush component. The brush has a sharp edge that can puncture tubing and cause user injury, and bristles may detach during use.
Megadyne Medical Products recalls its MEGA SOFT Universal Dual Patient Return Electrode due to reports of severe burn injuries, including third-degree burns requiring medical intervention. Use is now restricted to patients age 12 and older.
Sure Regular Antiperspirant Deodorant Aerosol (6 oz cans) sold nationwide in the US and Canada is being recalled due to benzene contamination. All lots expiring on or before August 2023 are affected.
Ineos Automotive Americas is recalling certain 2023–2024 Grenadier vehicles due to non-locking nuts that may have been installed on the steering rod ball joint, risking steering failure and loss of vehicle control.
Cake is recalling 2018-2023 Kalk motorcycles because lithium-ion battery cells can fail while charging, increasing the risk of a fire.
BlendJet Inc. is recalling approximately 4.8 million BlendJet 2 Portable Blenders because they can overheat, catch fire, or have blades that break off during use, creating fire and laceration hazards.
HMC Farms Nectarines 4lb bags are recalled due to potential Listeria monocytogenes contamination. The recall affects 26 US states, Mexico, Canada, and Taiwan.
HMC Farms Signature Farms Nectarines in 2lb bags are recalled due to potential Listeria monocytogenes contamination. The product was distributed across multiple U.S. states and to Mexico, Canada, and Taiwan.
ResMed is recalling AirFit F20 Full Face Masks due to magnets that can interfere with active medical implants. Updated warnings will guide safe distances for patients and those in close contact.
HMC Farms Peaches Signature Farms 2lb bags have been recalled due to potential Listeria monocytogenes contamination. The affected product was distributed widely across the United States and internationally.
HMC Farms Nectarines in 2lb gusset bags are being recalled due to potential Listeria monocytogenes contamination. The product has been distributed across the United States and internationally.
ResMed is recalling the AirFit F30i Full Face Mask due to potential magnetic interference with active medical implants and ferromagnetic objects. Safety warnings are being updated.
TGD Cuts, LLC is recalling Melon Loupe/Dew Chunks packaged in film due to potential Salmonella contamination. The affected product was distributed in nine northeastern and mid-Atlantic states.