PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: May 24, 2017 Initiated: May 15, 2017 #D-0788-2017

Product Description

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 for Recall

Lack of assurance of sterility: customer complaints received for the presence of leaks.

Details

Units Affected
113,590 bags
Distribution
US and foreign countries: United Arab Emirates, Colombia, and Canada
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
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. Recalled by Baxter Healthcare Corporation. Units affected: 113,590 bags.
Why was this product recalled?
Lack of assurance of sterility: customer complaints received for the presence of leaks.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 24, 2017. Severity: Moderate. Recall number: D-0788-2017.