Drug recall
Paroxetine 40mg Tablets USP; 90 Tablets NDC 0093-7121-98; Rx only. Manufactured in Israel By: Teva…
FDA recall event 49530 · Class II · Teva Pharmaceuticals USA, Inc.
Key facts
| Event ID | 49530 |
|---|---|
| Recall numbers | D-203-2009 |
| Recalling firm | Teva Pharmaceuticals USA, Inc. |
| Product type | Drugs |
| Products | Paroxetine 40mg Tablets USP; 90 Tablets NDC 0093-7121-98; Rx only. Manufactured in Israel By: Teva Pharmaceutical ind, ltd.,Jerusalem, 91010, Israel. Manufactured for: Teva pharmaceutical USA… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Superpotent; exceeds weight and potency requirements |
| Initiation date | Aug 27, 2008 |
| Termination date | Oct 9, 2009 |
| City | Sellersville |
| State | PA |
| Country | United States |
| FEI number | 2517175 |
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