# FDA recall Z-2599-2018

> **Beckman Coulter Inc.** · Class II · device recall initiated 2018-05-04.

## Product

MicroScan Pos Combo Panel Type 43, Catalog number B1017-217for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and Listeria monocytogenes.

## Reason for recall

The drug dilution sequence for Moxifloxacin printed on the panel is incorrect. As a result, incorrect MIC results for Mxf could be reported.

## Distribution

NJ, TX, IA, PA, FL, NE, OH, NY, CA, MO, OK, LA

## Key facts

- **Recall number:** Z-2599-2018
- **Recalling firm:** Beckman Coulter Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-04
- **Report date:** 2018-08-08
- **Termination date:** 2020-08-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brea, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2599-2018

## Citation

> AI Analytics. FDA recall Z-2599-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2599-2018. Source: US FDA. Licensed CC0.

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