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.
Keystone RV is recalling 2018 Crossroads Redwood and Cameo trailers because the propane manifold may contact the floor, potentially damaging the line and causing a leak that increases fire risk.
BMW is recalling 2014-2017 R NINE T motorcycles because swingarm pivot pin bolts may loosen, increasing crash risk. Dealers will repair the issue free of charge.
Mercedes-Benz is recalling 2016-2017 AMG GLE43 vehicles because software conflicts may cause the engine to shut down while driving, increasing crash risk.
Ride the Ducks is recalling 1996-2005 amphibious vehicles because the front axle housing may fracture, potentially causing a loss of vehicle control.
Forest River is recalling 2016-2017 Berkshire vehicles because an improperly installed battery cable bracket may cause chafing and short circuits, increasing fire risk.
Streetcar ORV LLC is recalling 2013-2017 RAM 2500 and 3500 trucks modified with specific cast aluminum wheels that may fracture, causing rapid air loss and potential loss of vehicle control.
Temsa is recalling 2014-2018 TS45 coach buses because the tag axle steering hydraulic hose may leak or burst, potentially causing loss of control or fire.
VistaPharm is recalling Lactulose Solution, USP, because the product failed microbial testing for yeast and mold counts.
Apace KY LLC is recalling Cyclobenzaprine HCl 5 mg tablets because cartons were mislabeled as Amantadine HCl 100 mg capsules.
Kenosha Beef International is recalling beef patties containing undeclared milk and bacon. The products were mislabeled as plain beef burgers.
Hospira is recalling specific lots of Sodium Bicarbonate 4% Additive Solution because they may lack sterility assurance. The recall covers 21.4 million vials distributed in the U.S. and internationally.
Hospira is recalling Quelicin (succinylcholine chloride) injection vials because they may lack sterility assurance. The recall covers 15,034,600 vials distributed in the U.S. and internationally.
Vi-Jon, Inc. is recalling 101,244 bottles of Magnesium Citrate Oral Solution because the product was found to contain mold identified as Rhinocladiella similis.
Woodstock Farms is recalling Nature's Promise Organic Campfire Trail Mix because a supplier's facility tested positive for Listeria monocytogenes.
United Natural Trading Inc. dba Woodstock Farms is recalling Market Basket Cape Cod Cranberry Mix 10oz. because a supplier found Listeria monocytogenes in their facility.
Myelotec, Inc. is recalling 2,980 Video Guided Catheters because a defective Access Port Body component can cause the port to become obstructed or blocked.
Newmar is recalling 2014-2017 Dutch Star and 2014 Mountain Aire recreational vehicles because a battery cable may short circuit, increasing the risk of a fire.
Clif Bar & Company is recalling Clif Kid Zbar Protein Chocolate Mint bars due to undeclared peanuts and/or tree nuts.
Hospira is recalling 20.3 million vials of Potassium Phosphates Injection because of a lack of sterility assurance. The product was distributed in the U.S. and several international locations.
Hospira is recalling 8.4% Sodium Bicarbonate Injection vials because they may lack sterility assurance. The recall covers 91,483,150 vials distributed in the U.S. and internationally.
Woodstock Farms is recalling Market Basket Fiber Frenzy 10oz. because a supplier found Listeria monocytogenes in their facility.
BMW is recalling 2012-2013 X3 and 2013 M6 vehicles because a defective driver's air bag inflator could cause metal fragments to strike occupants in a crash.
Chrysler is recalling 2017 Dodge Charger and Challenger vehicles with Hellcat engines because engine oil cooler hoses may fail, causing rapid oil loss and increased crash or fire risk.
Spartan Motors is recalling 2014-2017 Utilimaster Walk-In Vans because seat belt D-ring mountings may detach in a crash, increasing injury risk.
Hino is recalling 2018 NV8J, NJ8J, and NE8J trucks because door hinge bolts may be loose, allowing doors to open while driving.