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Class II: temporary or reversible health riskTerminated

Hospira Dextrose Injection Recall

Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc

Hospira Inc. · Lake Forest, IL

Risk level
Class II
Reported by FDA
Apr 27, 2016
Recall ID
D-0829-2016
Check your lot numberHow we source this data

Summary

Hospira recalled Dextrose Injection starting Mar 8, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0829-2016 on Apr 27, 2016. Reason: Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin. Status: Terminated.

Why it was recalled

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

Product description

Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7935-19, Barcode (01) 0 030409 793519 2

Lot numbers, UPCs & expiration codes

Lot# 52-114-JT, Exp 10/16

Where it was sold

US: Nationwide and Singapore

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0829-2016
Classification
Class II
Status
Terminated
Recall initiated
Mar 8, 2016
FDA report date
Apr 27, 2016
Quantity
552 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Hospira Inc.

Original FDA data

Every field from FDA enforcement report D-0829-2016, exactly as published.

Show all FDA fields
City
Lake Forest
State
IL
Status
Terminated
Country
United States
Event ID
73472
Address
275 N Field Dr
Code information
Lot# 52-114-JT, Exp 10/16
Postal code
60045-2579
Report date
Apr 27, 2016
Product type
Drugs
Recall number
D-0829-2016
Classification
Class II
Recalling firm
Hospira Inc.
Product quantity
552 bags
Termination date
Dec 6, 2017
Reason for recall
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Dextrose Injection, USP, 20%, Packaged as 500 mL in 1000 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7935-19, Barcode (01) 0 030409 793519 2
Distribution pattern
US: Nationwide and Singapore
Recall initiation date
Mar 8, 2016
Initial firm notification
Letter
Center classification date
Apr 21, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0829-2016, published Apr 27, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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