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.
Chrysler is recalling 2014 Ram ProMaster vans because the accelerator pedal may get stuck, causing uncontrolled acceleration.
ConAgra Foods is recalling 54,673 pounds of chicken noodle soup mislabeled as chicken with rice, failing to declare wheat and egg allergens.
Mitsubishi is recalling 2013 Outlander Sport vehicles with leather seats because improperly routed air bag wiring may prevent the driver's air bag from deploying in a crash.
Schwing America is recalling 2012-2013 concrete pump trucks because a specific potting compound in DC-DC converters can conduct electricity and cause fires.
Chrysler is recalling 2014 Ram ProMaster vehicles because a manufacturing tool may have damaged a brake hose, potentially causing fluid leakage and reduced braking performance.
PFP Enterprises is recalling approximately 15,865 pounds of beef products distributed in four states and Puerto Rico due to possible contamination with multiple non-O157 E. coli strains.
Kaffenbarger is recalling certain 2006-2013 International trucks because a specific DC-DC converter potting compound can conduct electricity and cause a fire.
PACCAR is recalling 2014 Kenworth T370 chassis with Eaton hybrid transmissions because software may cause unintended acceleration.
Britax is recalling B-Agile and BOB Motion strollers because the folding mechanism can amputate fingertips or break fingers.
Gree is expanding its recall to include GE-brand dehumidifiers that can overheat, smoke, and catch fire. Consumers should unplug the units and contact Gree for a refund.
Aidapak Services, LLC is recalling Tizanidine HCl 2 mg tablets that may have been mislabeled as Niacin TR 500 mg.
Aidapak Services, LLC is recalling Pyridoxine HCL 25 mg tablets because they may have been mislabeled as Torsemide 10 mg.
Codman & Shurtleff, Inc. is recalling 3,860 units of the TRUFILL n-BCA Liquid Embolic System due to incorrect instructions for use.
Aidapak Services, LLC is recalling Venlafaxine HCL 100 mg tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services is recalling 909 tablets of Hyoscyamine Sulfate SL 0.125 mg because they may have been mislabeled as other prescription drugs.
Aidapak Services, LLC is recalling Atorvastatin Calcium 10 mg tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services, LLC is recalling 10 mg Nortriptyline HCL capsules because they may have been mislabeled as 80 mg Valsartan tablets.
Aidapak Services, LLC is recalling 5 mg Escitalopram tablets because they may have been mislabeled as Sodium Chloride tablets.
Aidapak Services, LLC is recalling 200 mg Mexiletine HCL capsules that may have been mislabeled as 10 mg Isosorbide Dinitrate tablets.
Aidapak Services is recalling repacked progesterone capsules that may be mislabeled as levothyroxine sodium tablets. The error could lead to patients receiving the wrong medication.
Aidapak Services, LLC is recalling Minocycline HCL capsules that may have been mislabeled as Progesterone. The repacked drugs were distributed in four western states.
Aidapak Services is recalling Guanfacine HC tablets because they may have been mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.
Aidapak Services is recalling Levothyroxine Sodium 175 mcg tablets because they may have been mislabeled as other medications.
Aidapak Services is recalling 1 mg Sirolimus tablets that may be mislabeled as Propranolol or Hydrocortisone. The repacked drugs were distributed in four western states.
Aidapak Services is recalling Terbutaline Sulfate 2.5 mg tablets because they may have been mislabeled as Sotalol HCl 80 mg.