Drug recall
Morphine Sulfate in 5% Dextrose Injection, Each mL contains morphine sulfate pentahydrate 1mg and dextrose…
FDA recall event 28490 · Class II · ABBOTT Labs
Key facts
| Event ID | 28490 |
|---|---|
| Recall numbers | D-125-4 |
| Recalling firm | ABBOTT Labs |
| Product type | Drugs |
| Products | Morphine Sulfate in 5% Dextrose Injection, Each mL contains morphine sulfate pentahydrate 1mg and dextrose hydrous 50mg, 1 mg/mL (250 ml total) Large Volume Glass Container, Rx only, Abbott… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Sub-potent; product labeled as containing 1mg/mL of Morphine Sulfate actually contains 0.2mg/mL of Morphine Sulfate |
| Initiation date | Feb 24, 2004 |
| City | North Chicago |
| Country | United States |
| FEI number | 3001630466 |
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