Acetaminophen 325mg tablets — Class II drug recall D-0900-2017
Terminated recall by Safecor Health, LLC, reported 2017-06-21, distributed in MA, NY. CGMP Deviations
| Recall number | D-0900-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Safecor Health, LLC, Woburn, MA, United States |
| Recall initiated | 2016-07-07 |
| Classified | 2017-06-12 |
| Reported by FDA | 2017-06-21 |
| Terminated | 2017-07-12 |
| Distributed | MA, NY |
| Quantity | 66 bottles |
| Reason classes | cgmp |
| Lot numbers | A18688 |
| Expiration dates | 2018-09-30 |
Product
Acetaminophen 325mg tablets, 120-count bottles, Pk By Safecor Health Woburn, MA 01801, NDC 00904198280.
Reason for recall
CGMP Deviations
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-0900-2017. 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.