Drug recall
Nifedipine Extended Release Tablets, 30 mg, 100 tablets, Rx only, NDC 63739-451-10, Mfg by: Eurand, Inc…
FDA recall event 60747 · Class III · Mckesson Packaging Services
Key facts
| Event ID | 60747 |
|---|---|
| Recall numbers | D-1171-2012, D-1172-2012 |
| Recalling firm | Mckesson Packaging Services |
| Product type | Drugs |
| Products | Nifedipine Extended Release Tablets, 30 mg, 100 tablets, Rx only, NDC 63739-451-10, Mfg by: Eurand, Inc., Vandalia, OH 45377., Nifedipine Extended Release Tablets, 60 mg, 100 Tablets, NDC: 63739-452-10, Rx only, Mfg By: Eurand, Inc., Vandalia, OH 45377. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed USP Dissolution Test Requirements (below specification) |
| Initiation date | Dec 15, 2011 |
| Termination date | Jul 11, 2012 |
| City | Concord |
| State | NC |
| Country | United States |
| FEI number | 3000206187 |
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