US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 23, 2014 (12 years ago)

Fluconazole Injection, USP, 200 mg/100 mL (2 mg/mL), 100 mL Single-Dose INTRAVIA…

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

Why it was recalled

Lack of Assurance of Sterility: Complaints of leaks due to an incomplete seal at the bag seam.

What was recalled

Fluconazole Injection, USP, 200 mg/100 mL (2 mg/mL), 100 mL Single-Dose INTRAVIA Container bag, packaged in 10 x 100 mL Single Dose INTRAVIA container bags per carton, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-6046-48, Product Code 2J1446.

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-6046-48
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0380-2015

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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