FDA recall record

TRAVASOL 10%, Travasol (Amino Acid) Injection, 2000 ml, Pharmacy Bulk Package Not for Direct recall — FDA D-368-2014

Lack of Assurance of Sterility; Drug product leaking from container therefore sterility cannot be assured

Class IIclassification
D-368-2014official record ID
Dec 25, 2013report date

Recall record at a glance

Official recordD-368-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaxter Healthcare Corp.
Report dateDec 25, 2013
Recall initiation dateNov 12, 2013
Quantity14,622 bags
LocationDeerfield, IL, United States

Official product description

10%, Travasol (Amino Acid) Injection, 2000 ml, Pharmacy Bulk Package Not for Direct Infusion, Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield IL 60015 USA. NDC: 0338-0644-06.

Why the product was recalled

Lack of Assurance of Sterility; Drug product leaking from container therefore sterility cannot be assured

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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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