RecallRadar

FDA Drug recall D-0668-2016

Magnesium Sulfate in Water for Injection, (0.325 mEq Mg++/mL) 40 mg/mL, 2 g Total, 50 mL Single-Dose Container bag, Hospira, Inc., Lake For…

On 2016-02-24 the FDA classified a Class I recall of Magnesium Sulfate in Water for Injection, (0.325 mEq Mg++/mL) 40 mg/mL, 2 g Total, 50 mL Single-Dose Container bag, Hospira, Inc., Lake For… by Hospira, citing labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0668-2016
ClassificationClass I
Statusterminated
Initiated2016-01-05
Published2016-02-24
Last updated2026-09-13 11:51 UTC
CompanyHospira
DistributionUS

Product

Magnesium Sulfate in Water for Injection, (0.325 mEq Mg++/mL) 40 mg/mL, 2 g Total, 50 mL Single-Dose Container bag, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6729-24.

Reason

Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.

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: 53-113-JT, Exp 1NOV2016

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-0668-2016%22

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