Drug recall
Zyprexa tablets (olanzapine), 20 mg, 60 tablet bottles, Rx only. Eli Lilly & Co., Indianapolis, IN 46285
FDA recall event 27367 · Class II · Rochester Drug Cooperative Inc
Key facts
| Event ID | 27367 |
|---|---|
| Recall numbers | D-016-4 |
| Recalling firm | Rochester Drug Cooperative Inc |
| Product type | Drugs |
| Products | Zyprexa tablets (olanzapine), 20 mg, 60 tablet bottles, Rx only. Eli Lilly & Co., Indianapolis, IN 46285 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Counterfeit : An unknown number of bottles bearing these lot numbers are counterfeit, in that they have been repackaged, relabeled and/or may contain different strengths or mixed strength tablets… |
| Initiation date | Sep 22, 2003 |
| City | Rochester |
| Country | United States |
| FEI number | 1311675 |
At a glance
- 1–9 Products in this recall
- 1–9 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