🔍 RecallPedia

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.

Class I - Dangerous
💊 Drugs Recalled: April 5, 2012 Hospira Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Hospira, Inc.
Reason for Recall:
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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.

Product Codes/Lot Numbers:

Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1390-2012

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