Drug recall
Procardia XL (Nifedipine) Extended Release Tablets 30 mg, Rx only, 100 count (NDC 0069-2650-66) and 300 count…
FDA recall event 58597 · Class II · Pfizer Inc.
Key facts
| Event ID | 58597 |
|---|---|
| Recall numbers | D-827-2011 |
| Recalling firm | Pfizer Inc. |
| Product type | Drugs |
| Products | Procardia XL (Nifedipine) Extended Release Tablets 30 mg, Rx only, 100 count (NDC 0069-2650-66) and 300 count bottles (NDC 0069-2650-72), Distributed by Pfizer Labs, Division of Pfizer Inc., NY, NY |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specification |
| Initiation date | Apr 20, 2011 |
| Termination date | Sep 24, 2013 |
| City | New York |
| State | NY |
| Country | United States |
| FEI number | 2416101 |
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