Class II · Moderate riskOngoing Initiated Nov 11, 2024 (2 years ago)
Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
What was recalled
Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01
Recalling firm
Safecor Health, LLC
NDC code
48433-129-01
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0058-2025
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.