RecallRadar

FDA Drug recall D-1390-2012

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 F…

On 2012-06-27 the FDA classified a Class III recall of 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 F… by Hospira, citing superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1390-2012
ClassificationClass III
Statusterminated
Initiated2012-04-05
Published2012-06-27
Last updated2026-09-13 11:51 UTC
CompanyHospira
DistributionUS

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

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

Identifiers

ndc0409-6729-41
ndc0409-6729-23
ndc0409-6729-11
ndc0409-6729-24
ndc0409-4121-01
ndc0409-4121-24
ndc0409-2050-01
ndc0409-2050-20
ndc0409-3164-01
ndc0409-3164-12
ndc0409-5239-01
ndc0409-5239-24
code_infoLot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1390-2012%22

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