FDA Drug recall D-0780-2016
Fluconazole Injection, USP (in 0.9% Sodium Chloride), 200 mg per 100 ml, Single-Dose Container Bag, Rx only, Mfd. for SAGENT Pharmaceutical…
- FDA Drug
- Class II
- terminated
- Published 2016-03-30
On 2016-03-30 the FDA classified a Class II recall of Fluconazole Injection, USP (in 0.9% Sodium Chloride), 200 mg per 100 ml, Single-Dose Container Bag, Rx only, Mfd. for SAGENT Pharmaceutical… by Sagent Pharmaceuticals, citing cross contamination with other products: metronidazole.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0780-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-01 |
| Published | 2016-03-30 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Sagent Pharmaceuticals |
| Distribution | US |
Product
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
Reason
Cross contamination with other products: metronidazole
Identifiers
| code_info | Lot #: 40608, Exp 5/17 |
|---|
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-0780-2016%22
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