Drug recall
Premarin Tablets, (Conjugated Estrogens Tablets, USP), 0.625 mg, 100 tablet bottles, Rx Only, Manufactured by…
FDA recall event 26600 · Class III · McKesson
Key facts
| Event ID | 26600 |
|---|---|
| Recall numbers | D-295-3 |
| Recalling firm | McKesson |
| Product type | Drugs |
| Products | Premarin Tablets, (Conjugated Estrogens Tablets, USP), 0.625 mg, 100 tablet bottles, Rx Only, Manufactured by: Ayerst Laboratories, Inc. , A Wyeth-Ayerst Company, Philadelphia, PA 19101, Repackaged… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution Failure by the manufacturer (Wyeth) |
| Initiation date | May 20, 2003 |
| City | Memphis |
| Country | United States |
| FEI number | 3002568789 |
At a glance
- 1–9 Products in this recall
- None 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