FDA Drug recall D-0729-2021
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 799…
- FDA Drug
- Class II
- terminated
- Published 2021-08-25
On 2021-08-25 the FDA classified a Class II recall of Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 799… by Spirit Pharmaceuticals, citing cGMP deviations: Discolored acetaminophen.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0729-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-06-16 |
| Published | 2021-08-25 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Spirit Pharmaceuticals |
| Distribution | US |
Product
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10
Reason
cGMP deviations: Discolored acetaminophen
Identifiers
| code_info | Lot #: S210240, Exp. 03/2023 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0729-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.