Drug recall
Evista Tablets (Raloxifene HCl), 60 mg, 7 tablets blister pack, Rx Only, Eli Lilly and Company Indianapolis…
FDA recall event 26904 · Class III · Lilly, Eli & Co.
Key facts
| Event ID | 26904 |
|---|---|
| Recall numbers | D-331-3, D-342-3 |
| Recalling firm | Lilly, Eli & Co. |
| Product type | Drugs |
| Products | Evista Tablets (Raloxifene HCl), 60 mg, 7 tablets blister pack, Rx Only, Eli Lilly and Company Indianapolis, IN 46285, USA. NDC 0002-4165-01, Prozac Capsules Weekly (Fluoxetine Hydrochloride), Delayed Release Capsules, 90 mg fluoxetine, 4 capsules blister pack, Rx Only, Eli Lilly and Company Indianapolis, IN 46285 USA, NDC 0002-3004-75 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeling; Lot number and expiration date are not printed on the exterior carton labeling, Mislabeling; Lot number and expiration date are not printed on the external carton labeling |
| Initiation date | Aug 8, 2003 |
| City | Indianapolis |
| Country | United States |
| FEI number | 1819470 |
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