FDA recall record

Hospira Aminosyn II, 10%, Sulfite-Free Amino Acid Injection, 500 mL container recall — FDA D-461-2014

Presence of Particulate Matter: Confirmed customer complaint of particulate matter, identified as a human hair, visible in the injection port and primary…

Class Iclassification
D-461-2014official record ID
Jan 22, 2014report date

Recall record at a glance

Official recordD-461-2014
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHospira Inc.
Report dateJan 22, 2014
Recall initiation dateAug 30, 2013
Quantity17,256 containers
LocationLake Forest, IL, United States

Official product description

Aminosyn II, 10%, Sulfite-Free Amino Acid Injection, 500 mL container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4164-03, UPC (01) 0 030409 416403 8.

Why the product was recalled

Presence of Particulate Matter: Confirmed customer complaint of particulate matter, identified as a human hair, visible in the injection port and primary container.

Distribution information

Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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