Hospira, Inc. recalls Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, Rx only,

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Recalling firmHospira, Inc.600 N Field Dr Bldg J45, N/A · Lake Forest, IL 60045

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Brand
Hospira Inc.
Category
Drug

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Subject: Recall D-1390-2012 — Hospira Inc. Hospira, Inc. recalls Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg

Hello,

I own a Hospira, Inc. recalls Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, Rx only, that is covered by recall D-1390-2012 from Hospira Inc..

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-1390-2012 (April 5, 2012) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1390-2012 to see it in context.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.