Reported Jul 13, 2016 · Ongoing

Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25…

Hospira Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579

Is this the product you have?

    • Magnesium Sulfate Inj
    • USP 50%
    • 10 g/20 mL (0.5 g/mL)
    • (4 mEq Magnesium/mL
    • 20 mL Single-dose vial
    • packaged in 25 vials per box
    • Rx Only
    • Hospira
    • Inc
    • Lake Forest
    • IL 60045
    • NDC 0409-2168-02
    • barcode (01) 2 030409 216802 5
Lot codes and dates
  • Lot #: 50-343-DK*, Exp 01FEB2017; note that the lot number may be followed by numbers from 01 to 99.
Amount recalled
88,500 vials

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Presence of Particulate Matter: Confirmed customer complaint for the presence of particulate matter.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 5:53 PM UTC

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