US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 1, 2016 (11 years ago)

Fluconazole Injection, USP (in 0.9% Sodium Chloride), 200 mg per 100 ml, Single-Dose…

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

Why it was recalled

Cross contamination with other products: metronidazole

What was recalled

Fluconazole Injection, USP (in 0.9% Sodium Chloride), 200 mg per 100 ml, Single-Dose Container Bag, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195, NDC 25021-0113-82

Recalling firm
Sagent Pharmaceuticals Inc
NDC code
25021-0113-82
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0780-2016

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.

Other Chloride recalls

See all