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.

FDA recall notice · announced June 27, 2012 · Hospira

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

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.

Notes

Distribution: Nationwide
Lot/code information: Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
Quantity: 164,568 containers
Status: Terminated
Products in this recall event:
- 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. (D-1390-2012)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.