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.
Mercedes-Benz is recalling 2,563 AMG GLC63 vehicles because a starter cable may chafe and short-circuit, increasing the risk of a stall or fire.
Kawasaki is recalling 2021 Ninja 400 and Z400 motorcycles because a weak camshaft chain tensioner could cause the engine to stall, increasing crash risk.
Ohlins is recalling front struts for specific Porsche 911 models because the strut pin may break during maximum steering, potentially causing loss of vehicle control.
Yamaha is recalling 1,375 Skeeter boat trailers because improperly torqued brake caliper pins may dislodge, causing loss of braking and increasing crash risk.
Altec is recalling 2018-2020 digger derricks and aerial devices because a hydraulic check valve snap ring can fail, causing unintended boom movement.
Forest River is recalling certain 2020-2021 XLR Boost Toy Hauler recreational vehicles with inaccurate Federal Placards that may understate the vehicle's weight, risking tire damage and crashes from overloading.
Honda is recalling 2002-2006 CR-V vehicles because moisture in the driver-side power window switch may cause it to overheat, smoke, or catch fire.
Honda is recalling 2013-2015 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because a lubricant issue may cause drive shafts to break, risking loss of power or vehicle roll-away.
Honda is recalling specific 2007-2015 Acura and Honda models because improperly coated drive shafts may break, causing loss of power or vehicle roll-away.
Torrent Pharma Inc. is recalling 2,496 bottles of Anagrelide Capsules, USP 1 mg, because the product failed to meet dissolution specifications.
L G Sourcing is recalling allen + roth 62-inch electric fireplaces sold at Lowe's because wiring connectors can overheat, posing a fire hazard.
Invacare is recalling 384,767 PerfectO2 V oxygen concentrators worldwide due to a defect that may cause self-extinguishing fires or cap explosions.
CME America is recalling T34L PCA syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.
Medtronic is recalling MiniMed 640G insulin pumps because a missing solder battery connection could interrupt power. The recall covers specific serial numbers distributed in the U.S. and abroad.
Medtronic is recalling 391 MiniMed 670G insulin pumps because a missing solder battery connection could interrupt power to the device.
Tanimura & Antle is recalling specific lots of Romaine lettuce after Michigan state officials detected E. coli O157:H7 during routine sampling.
Audi is recalling 2,355 2018-2019 RS 5 Coupe vehicles because an incorrect positive battery terminal cover could prevent doors from opening or hazard lights from working after a rear crash.
CME America is recalling 4,182 NeoThrive syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.
Nissan is recalling 2020 Titan and Titan XD trucks because an exposed wire in the engine harness could cause an electrical short, leading to engine stall or fire.
Nissan is recalling specific Infiniti models because a broken driveshaft can cause loss of propulsion or disable the parking brake, increasing crash risk.
AA Products Inc. is recalling SYP Health Hand Sanitizer Alcohol Gel due to CGMP deviations and a history of subpotent ethanol and methanol contamination at the manufacturing facility.
Hill-Rom is recalling 67 Life2000 Ventilation Systems because they pose a risk of fire under certain conditions. The devices are used in home and institutional settings.
GT's Living Foods is recalling Synergy raw kombucha Multi-Green due to high levels of microcystins found by FDA sampling.
Kia is recalling 294,756 vehicles from 2011-2015 due to a risk of engine compartment fire while driving. Dealers will inspect for leaks and update software.
Sunstar Americas is recalling Paroex Oral Rinse due to microbial contamination with Burkholderia lata. The recall covers specific lots distributed nationwide.