Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 USA, NDC 0409-6729-03.
Reported: October 17, 2018 Initiated: October 3, 2018 #D-0015-2019
Product Description
Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 USA, NDC 0409-6729-03.
Reason for Recall
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found inside a case of Magnesium Sulfate in Water for Injection.
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 94,752 bags
- Distribution
- Nationwide in the USA and Puerto Rico
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 USA, NDC 0409-6729-03.. Recalled by Pfizer Inc.. Units affected: 94,752 bags.
Why was this product recalled? ▼
Correct Labeled Product Mispack: confirmed report involving a single unit of properly labeled Heparin in 0.45% Sodium Chloride for Injection (NDC 0409-7651-03, Lot 87903FW) that was found inside a case of Magnesium Sulfate in Water for Injection.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 17, 2018. Severity: Moderate. Recall number: D-0015-2019.
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