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.
Jayco is recalling 2020 motorized recreational vehicles because the adhesive on frameless windows may fail, allowing glass to detach and become a projectile.
Forest River is recalling 2021 Prime Time Avenger travel trailers because safety chains may be incorrectly attached, posing a risk of total trailer separation.
Ford is recalling specific 2011-2016 vehicles because previous door latch repairs may have been incomplete, potentially allowing doors to open while driving.
Ford is recalling 2014-2017 F-150 trucks with 3.5L engines because the brake master cylinder may leak fluid, increasing the risk of a crash.
Mercedes-Benz is recalling 2020 GLE 450, GLS 450, and GLS 580 4MATIC vehicles because leaking suspension components may affect handling and increase crash risk.
Mercedes-Benz is recalling 2020 E450, GLC300, and AMG models because the left-rear seatback latch may fail, increasing injury risk in a crash.
General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch striker wires may fracture, allowing the hood to open while driving.
Braun Ambulances is recalling 31 Demers ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
Quest Medical is recalling MPS Top Cover Replacement Kits because additive and arrest agent labels were swapped, posing a risk of over-delivering potassium during surgery.
Siemens is recalling 20 Cios Spin X-Ray systems because unplugging the monitor cable can create unsafe voltage, posing an electrical shock hazard.
Clinical Innovations is recalling 280 Clearview Total Uterine Manipulators (model UM750) because a missing notch on the tip support may prevent proper attachment of surgical components.
Biomet is recalling 15 units of Regenerex Series-A Patella knee prostheses due to potential endotoxin levels exceeding specifications.
Heartware, Inc. is recalling 2,225 HVAD Pump Implant Kits because the outflow graft may tear and the strain relief screw may break during pre-implant assembly.
Bentley is recalling 1,892 2019-2020 Bentayga vehicles because a fuel line connector may leak, increasing the risk of fire.
Keystone RV Company is recalling 2020 Springdale trailers because they were equipped with incorrect axles and tires, which may cause the trailer to be overloaded and increase the risk of a crash.
Vee Tyre is recalling 522 Taiga A/T tires because the sidewall may separate, increasing the risk of a crash.
Forest River is recalling 2020-2021 US Cargo, Haulin', and Trail & Sport cargo trailers because safety chains may break if the trailer becomes unhitched.
Braun Ambulances is recalling 2019 Chief XL and Liberty ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
Frazer is recalling 2019-2020 emergency vehicles on RAM 4500 and 5500 chassis because rear brake lines may wear, causing brake failure and increasing crash risk.
Thor Motor Coach is recalling 566 2020 motorhomes because a fender liner may chafe the brake hose, potentially causing brake fluid loss and increased braking distance.
Honda is recalling specific 2018-2020 models because a faulty fuel pump may cause the engine to stall while driving, increasing crash risk.
Nestle Prepared Foods is recalling Lean Cuisine Fettuccini Alfredo products because they contain undeclared soy and chicken, which are not listed on the label.
K2M, Inc. is recalling Aleutian Interbody Spacer Systems because the welded spreader tips may break off during spinal procedures.
ICU Medical Inc. is recalling 93,648 units of Lactated Ringer's Injection due to confirmed iron oxide particulate matter.
K2M, Inc. is recalling Aleutian Lordotic Spreaders because the welded tips may break off during spinal procedures.