Drug recall
Propafenone Hydrochloride Tablets, 225 mg, 100 Tablet bottles, Rx only Manufactured By: Watson Laboratories…
FDA recall event 51338 · Class I · Watson Laboratories Inc
Key facts
| Event ID | 51338 |
|---|---|
| Recall numbers | D-1212-2009 |
| Recalling firm | Watson Laboratories Inc |
| Product type | Drugs |
| Products | Propafenone Hydrochloride Tablets, 225 mg, 100 Tablet bottles, Rx only Manufactured By: Watson Laboratories, Inc. Corona, CA 92880 USA, NDC 0591-0583-01 |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some tablets may contain slightly higher levels of the active ingredient than specified. |
| Initiation date | Mar 10, 2009 |
| Termination date | Dec 23, 2010 |
| City | Corona |
| State | CA |
| Country | United States |
| FEI number | 2024830 |
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