Severity
Low
FDA Drug recall · Reported June 27, 2012
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Hospira, Inc. recalled Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL … - a low-severity action.
Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL … was recalled by Hospira, Inc. in June 27, 2012. Reason: Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.. Check the official notice for the remedy. Verify recall #D-1390-2012 with the FDA Drug before acting.
The recall
Hospira, Inc. issued this low-severity FDA Drug recall-Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate..
Sourced from official FDA Drug enforcement records. Verify recall #D-1390-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1390-2012) was formally reported on June 27, 2012, with the manufacturer initiating the action on April 5, 2012. It is classified under Low severity (Class III), with a current status of Terminated. Hospira, Inc. is listed as the recalling firm, operating out of Lake Forest, IL. Federal records list the affected scope as 164,568 containers.
The documented reason for this recall is: Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
164,568 containers
Related Recalls
6
5 from same agency
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.
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1390-2012 |
| Date reported | June 27, 2012 |
| Date initiated | April 5, 2012 |
| Recalling firm | Hospira, Inc. |
| Firm location | Lake Forest, IL |
| Affected scope | 164,568 containers |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported June 27, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.