Acetaminophen 325 mg tablets — Class II drug recall D-0729-2021
Terminated recall by Spirit Pharmaceuticals, reported 2021-08-25, distributed nationwide. cGMP deviations: Discolored acetaminophen
| Recall number | D-0729-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spirit Pharmaceuticals, Ronkonkoma, NY, United States |
| Recall initiated | 2021-06-16 |
| Classified | 2021-08-16 |
| Reported by FDA | 2021-08-25 |
| Terminated | 2022-09-07 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| NDC | 79903-0052-10 |
| Lot numbers | S210240 |
| Expiration dates | 2023-03 |
Product
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10
Reason for recall
cGMP deviations: Discolored acetaminophen
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-0729-2021. 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.