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Class II: temporary or reversible health riskTerminated

Hospira Aminosyn-PF Recall

Aminosyn-PF (amino acids) 7%, Sulfite-Free, 500 mL Bags, Rx Only, Hospira, Inc

Hospira Inc. · Lake Forest, IL

Risk level
Class II
Reported by FDA
Apr 27, 2016
Recall ID
D-0830-2016
Check your lot numberHow we source this data

Summary

Hospira recalled Aminosyn-PF starting Mar 8, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0830-2016 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

Aminosyn-PF (amino acids) 7%, Sulfite-Free, 500 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-4178-03 Barcode (01) 0 030409 417803 5

Lot numbers, UPCs & expiration codes

Lot# 49-047-JT, Exp: 07/16

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-0830-2016
Classification
Class II
Status
Terminated
Recall initiated
Mar 8, 2016
FDA report date
Apr 27, 2016
Quantity
1776 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Hospira Inc.

Original FDA data

Every field from FDA enforcement report D-0830-2016, 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# 49-047-JT, Exp: 07/16
Postal code
60045-2579
Report date
Apr 27, 2016
Product type
Drugs
Recall number
D-0830-2016
Classification
Class II
Recalling firm
Hospira Inc.
Product quantity
1776 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
Aminosyn-PF (amino acids) 7%, Sulfite-Free, 500 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-4178-03 Barcode (01) 0 030409 417803 5
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-0830-2016, 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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