Aspirin Chewable tablet 81 mg — Class II drug recall D-0058-2025
Ongoing recall by Safecor Health, LLC, reported 2024-11-27, distributed nationwide. cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
| Recall number | D-0058-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Safecor Health, LLC, Woburn, MA, United States |
| Recall initiated | 2024-11-11 |
| Classified | 2024-11-19 |
| Reported by FDA | 2024-11-27 |
| Distributed | Nationwide (US) |
| Quantity | 1,470 boxes |
| Reason classes | cgmp |
| NDC | 48433-0129, 48433-0129-01 |
| Lot numbers | 24A0061 |
| Expiration dates | 2026-05-23 |
Product
Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01
Reason for recall
cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0058-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.