Drug recall
Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container…
FDA recall event 62053 · Class III · Hospira, Inc.
Key facts
| Event ID | 62053 |
|---|---|
| Recall numbers | D-1390-2012 |
| Recalling firm | Hospira, Inc. |
| Product type | Drugs |
| Products | Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, Rx only, Hospira, Inc., Lake Forest, IL 60045; NDC 0409-6729-24. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate. |
| Initiation date | Apr 5, 2012 |
| Report date | Jun 27, 2012 |
| Termination date | Aug 8, 2013 |
| 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 · Source date: