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.
Zydus Pharmaceuticals is recalling Carvedilol 6.25 mg tablets because one bottle was found labeled as Acyclovir 400 mg.
Sagent Pharmaceuticals is recalling 75,825 vials of Ketorolac Tromethamine Injection because microbial growth was detected during a routine manufacturing simulation.
Crab House Trading Corp. is recalling approximately 49,000 pounds of frozen yellow walking fish produced without federal inspection.
Oregon's Wild Harvest is recalling dried whole elderberry products due to glass fragment contamination. The recall affects 4 oz and 1 lb bags distributed in 23 states.
Navistar is recalling 2019 International CV trucks with Duramax 6.6L diesel engines and optional block heaters due to a short-circuit risk that could cause a fire.
Daimler Trucks North America is recalling 253 specific 2019 heavy-duty trucks because brake caliper mounting bolts may be insufficiently tightened, potentially reducing brake effectiveness.
Daimler Trucks North America is recalling 2019 Thomas Built Buses Saf-T-Liner C2 vehicles because loose brake caliper bolts may reduce braking effectiveness.
Daimler Trucks North America is recalling 741 Freightliner, Sterling, and Western Star trucks because insufficient air reservoir capacity may reduce brake effectiveness and increase crash risk.
Daimler Trucks North America is recalling 2012-2019 Freightliner Custom Chassis MT55 and MT45 vehicles because a brake pedal clip may detach, causing brake light failure or pedal detachment.
Autocar is recalling 2019-2020 Xpeditor vehicles because the rear axle brake may have a delayed release, increasing crash risk.
LDJ Manufacturing is recalling 102 2019 Thunder Creek trailers because wheel lug nuts may loosen, potentially causing a wheel to separate and increasing crash risk.
Ford is recalling 2019 Ranger vehicles because transmission shifter cable bracket fasteners may loosen, causing the gear indicator to mismatch the actual gear and increasing crash risk.
Trail King is recalling 2016-2019 TKT50 trailers because a missing air control line may prevent service brakes from applying on some axles, increasing crash risk.
Spartan Motors is recalling 2018-2020 emergency response and motor home chassis because a brake relay valve defect may increase stopping distance.
Ford is recalling 2013-2016 Fusion vehicles with 2.5-liter engines because a transmission shifter cable bushing may degrade and detach. This could allow the driver to exit the vehicle while the transmission is not in Park, increasing crash risk.
Forest River is recalling 2019-2020 R-POD travel trailers because a refrigerator wire may be connected to a breaker that allows too much current, increasing the risk of fire.
Chrysler is recalling specific Ram 1500, 2500, and 3500 pickup trucks because a tailgate latch component may fracture, causing the tailgate to open while driving and creating a road hazard.
Jaguar Land Rover is recalling 2016-2017 Range Rover and Range Rover Sport vehicles because the driver's seat belt may not lock properly during braking, increasing injury risk.
BMW is recalling 2016-2019 X1 vehicles because the B-pillar may not absorb impact adequately in a crash, increasing injury risk.
Jaguar is recalling 2019-2020 I-PACE vehicles because a regenerative brake failure can delay deceleration, increasing crash risk.
Chrysler is recalling 2017-2019 Pacifica vehicles with stop/start systems because a loose battery ground connection may cause power steering loss or stalling, increasing crash risk.
Customceutical Compounding is recalling 8 vials of Test D compounded injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 100 mg, because FDA labs confirmed the presence of the impurity NMBA above acceptable levels.
Philips is recalling Fetal Spiral Electrodes because the metal tip may break off and remain in a newborn's scalp during delivery.
Torrent Pharma Inc. is recalling Losartan Potassium Tablets because FDA labs found an impurity above acceptable levels.