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.
Motor Coach Industries is recalling 2014-2019 J4500 and 2018-2019 J3500 motor coaches because brake hoses may crack, causing air leaks and increased stopping distances.
Blue Bird is recalling 2006-2021 Vision and 2007-2013 All American school buses because the parking brake may fail to hold the vehicle on an incline.
Blue Bird is recalling 2009-2019 Vision transit buses because the floor-mounted parking brake may fail to hold the vehicle on an incline when fully loaded.
McLaren is recalling 2,763 vehicles because a foam pad may corrode the fuel tank, potentially causing a leak and fire risk.
Ducati is recalling 97 2017 Superleggera motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.
Leviton is recalling approximately 98,000 50-ampere electrical connectors, plugs, receptacles, and inlets sold in the US and Canada due to mislabeled terminal markings that pose an electrical shock hazard.
Navistar is recalling 2019 International WorkStar and HV vehicles because insufficient axle lubrication may damage wheel bearings, potentially causing wheel separation and loss of vehicle control.
Lode-King is recalling 2015-2021 Prestige SDG53-2 step-deck semi-trailers because cargo winch mounts may fail, allowing cargo to fall off and create road hazards.
Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 25 mg because an impurity, NBMA, was detected in the active ingredient.
Sysmex America is recalling 40 CV-11 Sample Units because urine spills on the transport track can reach electrical components, creating a potential for smoke, sparks, and combustion.
The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to lack of processing control. The product was distributed in Florida.
The Medicine Shoppe Pharmacy is recalling Levothyroxin/Liothyronine SR capsules due to a lack of processing control. The affected product was distributed in Florida.
Abbott is recalling the Merlin PCS 3650 Software Upgrade Kit because a software anomaly may cause the device to use a previously programmed shock energy level without alerting the user.
Aurobindo Pharma USA Inc. is recalling specific lots of Gabapentin Capsules because they were manufactured in an area with observed water leakage.
Altec is recalling 92 ST Spray Trucks from 2017-2020 because an improperly mounted battery fuse holder may cause an electrical short circuit and fire.
TransitWorks is recalling 2019-2020 Ford Transit and RAM ProMaster vans because seat belt retractors may not secure occupants properly.
LDJ is recalling 2018-2019 Thunder Creek Multi-Tank Upfits because adhesive securing the chassis filler may fail, risking load movement and crashes.
Eldorado is recalling 2018-2020 CNG-powered vehicles because the pressure relief device may fail to vent heat, potentially causing the fuel system to rupture.
Navistar is recalling 2017-2020 International DuraStar and WorkStar models, plus IC bus vehicles with Cummins B6.7 engines. The electric fuel heater may overheat and catch fire or cause engine stalling.
Navistar is recalling 2017-2021 IC Bus CE school buses because the electric fuel heater may overheat, melt plastic, and cause a fire or engine stall.
Polaris is recalling approximately 80,000 Model Year 2018-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles because a broken clutch belt can damage the fuel line and cause a fire.
Teva Pharmaceuticals USA is recalling bulk Losartan Potassium Tablets 100 mg because an impurity called NMBA was detected in the active ingredient.
Zeiss is recalling a component for LSM 700, 800, and 900 microscopes because tilting the light arm can bypass laser safety, causing Class IIIB laser radiation emission.
Innovative Compounding Pharmacy is recalling Alprostadil, Papaverine, and Phentolamine injection due to a lack of assurance of sterility. The product was distributed to patients in California, Maine, and Texas.
PharMEDium Services is recalling 375 units of ePHEDrine Sulfate IV syringes because of a lack of sterility assurance.