Drug recall
Lisinopril Tablets USP, 30 mg, 100 count plastic bottles, Rx only, Manufactured for: Lupin Pharmaceuticals…
FDA recall event 58195 · Class II · Lupin Pharmaceuticals Inc.
Key facts
| Event ID | 58195 |
|---|---|
| Recall numbers | D-418-2011 |
| Recalling firm | Lupin Pharmaceuticals Inc. |
| Product type | Drugs |
| Products | Lisinopril Tablets USP, 30 mg, 100 count plastic bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Goa 403 722 India, NDC… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Adulterated Presence of Foreign Tablets: Product may contain foreign tablets. |
| Initiation date | Feb 15, 2011 |
| Termination date | Aug 17, 2012 |
| City | Baltimore |
| State | MD |
| Country | United States |
| FEI number | 3004097115 |
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