US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 25, 2014 (12 years ago)

Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility; leaks were observed from the bag seam and port seal

What was recalled

Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injections, in CLARITY Dual Chamber Container, Baxter Healthcare Corporation, Deerfield, IL NDC 0338-1115-04

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-1115-04
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0301-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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