D-1390-2012 Class III Terminated

Recalled by Hospira, Inc. — Lake Forest, IL

FDA drug recall D-1390-2012 was initiated by Hospira, Inc. on Apr 5, 2012 and is designated Class III. Reason for recall: Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate. The recall status is terminated (terminated Aug 8, 2013). Affected quantity: 164,568 containers.

Recall Details

Product Type
Drugs
Report Date
Jun 27, 2012
Initiation Date
Apr 5, 2012
Termination Date
Aug 8, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
164,568 containers

Product Description

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.

Reason for Recall

Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.

Distribution Pattern

Nationwide

Code Information

Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-1390-2012
openFDA file date
Oct 27, 2026
Loaded by RegDataLab
Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.