5% Dextrose and 0.45% Sodium Chloride Injection recall: Sterility Concern
5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC…
Why was 5% Dextrose and 0.45% Sodium Chloride Injection recalled?
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.
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 # 33-095-JT; Exp. 09/15 Lot # 36-030-JT; Exp. 12/15
- Product
- 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC…
- Recalling firm
- Hospira Inc.
- Quantity
- 823,296 bags
- Distribution
- Nationwide, Puerto Rico, and U.S. Virgin Islands.
- Recall date
- December 3, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)