RecallRadar

FDA Drug recall D-0206-2017

Fluconazole Injection, USP, 200 mg/100 mL (2mg/mL), 100 mL Single-Dose Intravia Container bag, Rx only, Baxter Healthcare Corporation, Deer…

On 2016-12-28 the FDA classified a Class II recall of Fluconazole Injection, USP, 200 mg/100 mL (2mg/mL), 100 mL Single-Dose Intravia Container bag, Rx only, Baxter Healthcare Corporation, Deer… by Baxter Healthcare, citing lack of Assurance of Sterility: confirmed customer complaints of leaking bags.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0206-2017
ClassificationClass II
Statusterminated
Initiated2016-12-06
Published2016-12-28
Last updated2026-09-13 11:51 UTC
CompanyBaxter Healthcare
Distributionn/a

Product

Fluconazole Injection, USP, 200 mg/100 mL (2mg/mL), 100 mL Single-Dose Intravia Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product Code 2J1446, NDC 0338-6046-48.

Reason

Lack of Assurance of Sterility: confirmed customer complaints of leaking bags.

Identifiers

ndc0338-6046-48
ndc0338-6045-37
code_infoLot #: P344028 on bags, P344028A on shipping container, Exp 12/31/2017

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0206-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.