Normosol-M and 5% Dextrose recall: Labeling Error
Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc.…
Why was Normosol-M and 5% Dextrose recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer report of an incorrect expiration date printed on the primary container labeled "01AUG1017" rather than "01AUG2017".
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 #: 56-853-FW, Exp 01AUG2017
- Product
- Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc.…
- Recalling firm
- Hospira Inc.
- Quantity
- 10,778 bags
- Distribution
- Nationwide and Hong Kong
- Recall date
- March 2, 2016
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)