Drug recall
Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc…
FDA recall event 88322 · Class II · Spirit Pharmaceuticals
Key facts
| Event ID | 88322 |
|---|---|
| Recall numbers | D-0729-2021 |
| Recalling firm | Spirit Pharmaceuticals |
| Product type | Drugs |
| Products | Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | cGMP deviations: Discolored acetaminophen |
| Initiation date | Jun 16, 2021 |
| Report date | Aug 25, 2021 |
| Termination date | Sep 7, 2022 |
| City | Ronkonkoma |
| State | NY |
| Country | United States |
| FEI number | 3011773798 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: