Drug recall
Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457…
FDA recall event 90790 · Class II · Padagis US LLC
Key facts
| Event ID | 90790 |
|---|---|
| Recall numbers | D-1497-2022 |
| Recalling firm | Padagis US LLC |
| Product type | Drugs |
| Products | Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed By Perrigo, Allegan, MI 49010, NDC 45802-064-36. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness. |
| Initiation date | Aug 17, 2022 |
| Report date | Sep 7, 2022 |
| Termination date | Sep 28, 2023 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 2127022 |
At a glance
- 1–9 Products in this recall
- 10–99 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: