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.
Life Science Pharmacy Inc. is recalling compounded Estriol capsules nationwide due to potential penicillin cross-contamination.
Western Drug is recalling Sal-Acid 60% Plaster Paste because the company cannot guarantee the product is sterile. The recall covers all lots distributed nationwide.
Western Drug is recalling 36 containers of Tri-Amino OAC 1:1:1 300mg/mL because the product lacks assurance of sterility.
Life Science Pharmacy Inc. is recalling TRI-EST Liquids because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
VRVK Nutraceuticals is recalling Dr. Venessa's Formulas Ultimate Antioxidant Tablets because FDA inspection found undeclared milk and crustacean shellfish.
Philips Medical Systems is recalling 14 Allura Xper Cardio systems because the monitor ceiling suspension system may fall.
Western Drug is recalling all lots of Progesterone Cyp Inj because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Dextrose 50% Injection Solution because there is a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling HCG 1000unit/10mL vials nationwide because the company cannot ensure the product is sterile.
Western Drug is recalling 41 containers of 17-Hydroxyprogesterone 250mg/mL Injection because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Sodium Chloride 0.9% Injections because the agency could not ensure the product was sterile. The recall covers all lots distributed nationwide.
Western Drug is recalling Hydroxocobalamin 1mg/mL Injection because the product lacks assurance of sterility. The recall covers three containers distributed nationwide.
Western Drug is recalling Gent 80 mg/Liter Nasal spray because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling 75 containers of Test Cyp/Test Prop 1:1 Injection due to a lack of assurance of sterility.
Western Drug is recalling Glutathione 300 mg/1.5 mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug Inc. is recalling Methylcobalamin Injection because the product lacks assurance of sterility. The recall affects 34 containers distributed nationwide.
Western Drug is recalling Ace-Promazine 10 mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Ascorbic Acid 500 mg/mL Injection because the product lacks assurance of sterility. The recall covers six containers distributed nationwide.
Western Drug is recalling Phenylephrine 500mcg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Heparin Sodium 30,000U/30ML Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling 45 containers of Sermorelin Injection because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Testost CYP 200mg/mL SUS due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling M-Cobalamin (B12) injections because the FDA determined there is a lack of assurance of sterility. The recall affects 3 containers distributed nationwide.
Western Drug is recalling Prostin Injection due to a lack of assurance of sterility. The recall covers 16 containers distributed nationwide.
Western Drug Inc. is recalling 17 containers of Medroxyprogesterone 150/LID 5 mg/mL Injection because the company cannot ensure the product is sterile.