Drug recall
Procainamide Hydrochloride Injection, USP, 1 gram/10 mL vial, Rx Only, NDC 0409-1902-01, Hospira, Inc. Lake…
FDA recall event 49588 · Class III · Hospira, Inc.
Key facts
| Event ID | 49588 |
|---|---|
| Recall numbers | D-019-2009 |
| Recalling firm | Hospira, Inc. |
| Product type | Drugs |
| Products | Procainamide Hydrochloride Injection, USP, 1 gram/10 mL vial, Rx Only, NDC 0409-1902-01, Hospira, Inc. Lake Forest, IL 80045 USA |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Discoloration of the solution which does not meet specification for color. |
| Initiation date | May 7, 2008 |
| Termination date | Jun 29, 2010 |
| City | Lake Forest |
| State | IL |
| Country | United States |
| FEI number | 3003940565 |
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