Drug recall
Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue…
FDA recall event 96907 · Class II · Aurobindo Pharma USA Inc
Key facts
| Event ID | 96907 |
|---|---|
| Recall numbers | D-0471-2025 |
| Recalling firm | Aurobindo Pharma USA Inc |
| Product type | Drugs |
| Products | Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N., Seattle, WA 98109, NDC 72288-405-10 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets). |
| Initiation date | May 22, 2025 |
| Report date | Jun 25, 2025 |
| City | East Windsor |
| State | NJ |
| Country | United States |
| FEI number | 3008460374 |
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: