# FDA recall D-1234-2015

> **Fresenius Kabi USA, LLC** · Class II · drug recall initiated 2015-06-04.

## Product

Rifampin for Injection, USP 600mg/vial in a 20mL vial, Rx only, Manufactured for Fresenius Kabi LLC 3 Corporate Drive, Lake Zurich, IL, 60047, by Fresenius Kabi LLC, 2020 N Ruby Street, Melrose Park, IL 60160. NDC 63323-351-20

## Reason for recall

Failed Impurities/Degradation Specifications; out-of-specification for color, impurity, and degradation

## Distribution

Nationwide,Hawaii, and Puerto Rico

## Key facts

- **Recall number:** D-1234-2015
- **Recalling firm:** Fresenius Kabi USA, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-06-04
- **Report date:** 2015-07-22
- **Termination date:** 2016-05-19

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1234-2015

## Citation

> AI Analytics. FDA recall D-1234-2015. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-1234-2015. Source: US FDA. Licensed CC0.

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