Drug recall
PREMARIN 0.625 mg (Conjugated Estrogens Tablets, USP), 100 tablet bottles, Rx Only, Manufactured by: Wyeth…
FDA recall event 31135 · Class III · Rx PAK
Key facts
| Event ID | 31135 |
|---|---|
| Recall numbers | D-131-5 |
| Recalling firm | Rx PAK |
| Product type | Drugs |
| Products | PREMARIN 0.625 mg (Conjugated Estrogens Tablets, USP), 100 tablet bottles, Rx Only, Manufactured by: Wyeth Pharmaceuticals Inc., Philadelphia, PA 19101; Repackaged by RxPak, Div of McKesson Corp… |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution Failure |
| Initiation date | Oct 28, 2004 |
| City | Memphis |
| Country | United States |
| FEI number | 3002574153 |
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