Drug recall
Metformin Hydrochloride Tablets 1000 mg, 60 Count bottles, NDC 0781-5052-61, Sandoz Inc., Princeton, NJ 08540.
FDA recall event 57991 · Class III · Sandoz Incorporated
Key facts
| Event ID | 57991 |
|---|---|
| Recall numbers | D-453-2011 |
| Recalling firm | Sandoz Incorporated |
| Product type | Drugs |
| Products | Metformin Hydrochloride Tablets 1000 mg, 60 Count bottles, NDC 0781-5052-61, Sandoz Inc., Princeton, NJ 08540. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Adulterated Presence of Foreign Tablets; Metformin HCl 500mg tablets may have been packaged with Metformin HCl 1000mg tablets. |
| Initiation date | Feb 24, 2011 |
| Termination date | Jul 13, 2011 |
| City | Broomfield |
| State | CO |
| Country | United States |
| FEI number | 1717759 |
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