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.
Whole Foods Market is recalling approximately 234 pounds of curry chicken salad products in five states due to possible Listeria monocytogenes contamination.
Honda is recalling specific GL1800, GL1800A, and GL1800B motorcycles because the rear brakes may drag after release, increasing the risk of a crash or fire.
Starcraft RV is recalling 36 model year 2016 Autumn Ridge trailers because unprotected propane lines and wires may be damaged by road debris, increasing the risk of fire.
Honda is recalling 25,367 2015-2016 Fit LX vehicles because defective rear grab handle brackets may puncture side curtain airbags, increasing injury risk in a crash.
Thor Motor Coach is recalling 2016 Challenger, Hurricane, and Windsport motorhomes because the parking brake may fail to hold the vehicle or disengage properly.
Navistar is recalling specific 2016 International ProStar and TranStar trucks because the transmission may lock or cause unexpected backward movement.
Thor Motor Coach is recalling specific Four Winds motorhomes because a transfer switch may overheat and cause a fire.
Toyota is recalling specific 2006-2011 models because inconsistent lubricant on the power window switch may cause overheating and fire.
Rustico Foods is recalling approximately 2,659 pounds of packaged soup products produced without the benefit of federal inspection. The products were shipped to retail establishments in southern California.
Shuler Meats is recalling approximately 25,920 pounds of fully cooked smoked turkey legs that were reconditioned without the benefit of FSIS inspection.
Mack Trucks is recalling 2014 Granite trucks because improperly tightened hex nuts on the drive axle may cause the driveshaft to disconnect, increasing crash risk.
United States Stove Company is recalling about 4,400 HomComfort 2400 pellet stoves because the internal fire box baffle can degrade and overheat, posing a fire hazard.
Bedford Pharmacy is recalling P-P (COBAL) 300-30/mL injections because there is a lack of assurance of sterility. The affected product was distributed in New Hampshire and Massachusetts.
Bedford Pharmacy is recalling four vials of P-P (COBAL) 30-2 /mL Injection because of a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.
Bedford Pharmacy is recalling P-P-P (COBAL) 30-4-40/mL Injection vials because there is a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.
Synthes (USA) Products LLC is recalling 1,550 Inserter for Titanium Elastic Nails (TEN) devices due to a potential for mechanical failures such as breakage.
Bedford Pharmacy is recalling Methylcobalamin 1 mg/mL Injection because there is a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.
Spartan Motors is recalling 2009-2014 Gladiator and MetroStar vehicles because power steering fluid may overheat, causing the steering to lock unexpectedly.
Bentley is recalling certain 2012-2015 Continental GT, GTC, and Flying Spur vehicles because a loose battery cable connection may overheat and cause a fire.
Bedford Pharmacy is recalling 4 vials of P-P-P (COBAL) 30-1-20/mL Injection due to a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.
Bedford Pharmacy is recalling Hydroxocobalamin 20 mg/mL Injection due to a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.
Bedford Pharmacy is recalling Testosterone Cypionate injections due to a lack of assurance of sterility. The affected products were distributed in New Hampshire and Massachusetts.
Nephron Pharmaceuticals is recalling Ipratropium Bromide and Albuterol Sulfate inhalation solution due to a lack of assurance of sterility.
Apotex Inc. is recalling specific lots of Bromfenac Ophthalmic Solution 0.09% because preservative testing failed, raising concerns about sterility.
Bedford Pharmacy is recalling P-P (COBAL) 30-0.5/mL injections because there is a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.