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.
Biota Biosciences is recalling sterile cannabidiol vials because they may not be sterile and were marketed without FDA approval.
NOW Health Group is recalling 4,251 bags of Raw Macadamia Nuts because the product tested positive for Salmonella enterica.
Volvo is recalling specific 2007-2020 models because a front seat belt cable may fatigue and fail to secure occupants during a crash.
FCA US LLC is recalling specific MOPAR steering drag link assemblies for Heavy Duty Ram 2500 and 3500 trucks because a jam nut may loosen, risking loss of steering control.
Tenneco is recalling Clevite-Pullman rear suspension lower control rods installed in Gillig Low Floor buses because the design makes them susceptible to failure over time.
Chrysler is recalling 2020 Ram 1500 pickups and Promaster vans because a side curtain airbag diffuser may detach, preventing proper inflation in a crash.
GE Healthcare is recalling Giraffe OmniBed infant incubators equipped with Servo Oxygen modules because they may deliver a different oxygen level than displayed.
PD-Rx Pharmaceuticals is recalling specific lots of metformin HCL ER 500 mg tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Brake Parts Inc. is recalling aftermarket brake master cylinders for specific Volkswagen models because the piston may pop out, risking a complete loss of braking.
Defibtech is recalling 860 Lifeline PRO AEDs because a component issue may cause the device to abort or fail to deliver a shock.
SCA Pharmaceuticals is recalling 333 bags of Heparin Sodium 5,000 units due to out-of-specification potency results at the 30-day stability timepoint.
Apotex Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
AvKARE Inc. is recalling Metformin Hydrochloride Extended-Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.
Forest River is recalling 2020 Palomino Real-Lite campers because window glass may detach from the frame, posing a projectile hazard.
Captain Rusty's Seafood Products LLC is recalling Lobster Dip because routine inspection found undeclared major allergens, including fish, egg, soy, milk, wheat, and crustacean shellfish.
Toyota is recalling 2013-2015 Prius and 2014-2017 Prius V vehicles because excessive voltage in the inverter may cause the hybrid system to shut down, increasing crash risk.
Triple E is recalling 2020 Wonder W24MB, W24RTB, and W24FTB motorhomes because an improperly tightened electrical connection may short circuit and cause a fire.
Ford is recalling 2020 F-250, F-350, and F-550 Super-Duty diesel pickups because a brittle transmission part may fracture, causing engine stalls or increased braking effort.
Newell is recalling 2020-2021 P50 motor coaches because a decorative cover may become lodged under the brake pedal, potentially impacting the ability to stop.
Mercedes-Benz is recalling 2020 C300, E350, and GLC300 vehicles because improperly tightened turbocharger oil line screws may cause leaks that increase fire risk.
Lochinvar is recalling about 34,300 residential boilers because a flue grommet can fail, allowing carbon monoxide to escape. Consumers should contact a technician for a free repair.
Volkswagen is recalling one 2020 Jetta because front brake caliper bolts may come loose, potentially affecting brake performance and increasing crash risk.
Rexair is recalling about 38,000 Rainbow SRX vacuums because the circuit board can spark, posing fire and burn hazards. Two fires have been reported.
Arrow International is recalling FlexTip Plus Epidural Kits because a rotatable collar on the filter may detach, causing a leak.
RaySearch Laboratories is recalling RayStation 5 Service Pack 3 software due to a dose calculation error that may underestimate radiation dose.