Magnesium Sulfate in Water for Injection recall: Labeling Error
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…
Why was Magnesium Sulfate in Water for Injection recalled?
Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: 53-113-JT, Exp 1NOV2016
- 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…
- Recalling firm
- Hospira Inc.
- Quantity
- 213,600 bags
- Distribution
- Nationwide
- Recall date
- February 24, 2016
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)