FDAClass IIApril 27, 2016

Dextrose Injection recall: Contamination

Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7936-19, Barcode (01) 0 030409 793619 9

Why was Dextrose Injection recalled?

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

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 # 52-002-JT, Exp 04/17

Product
Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7936-19, Barcode (01) 0 030409 793619 9
Recalling firm
Hospira Inc.
Quantity
4368 bags
Distribution
US: Nationwide and Singapore
Recall date
April 27, 2016
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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