# FDA recall D-0780-2016

> **Sagent Pharmaceuticals Inc** · Class II · drug recall initiated 2016-03-01.

## 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 for recall

Cross contamination with other products: metronidazole

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-0780-2016
- **Recalling firm:** Sagent Pharmaceuticals Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-03-01
- **Report date:** 2016-03-30
- **Termination date:** 2017-09-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Schaumburg, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0780-2016

## Citation

> AI Analytics. FDA recall D-0780-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0780-2016. Source: US FDA. Licensed CC0.

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