# FDA recall Z-2874-2018

> **Biomerieux Inc** · Class II · device recall initiated 2018-01-23.

## Product

bioM¿rieux VITEK 2 NH ID Test Kit    Product Usage:  Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria and yeast.

## Reason for recall

Missing desiccant.

## Distribution

US Nationwide Distribution in the states of AK, AL, AR, AZ, CA, CO, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT. VA. VT. WA. WI, and WV

## Key facts

- **Recall number:** Z-2874-2018
- **Recalling firm:** Biomerieux Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-23
- **Report date:** 2018-08-29
- **Termination date:** 2021-07-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hazelwood, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2874-2018

## Citation

> AI Analytics. FDA recall Z-2874-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2874-2018. Source: US FDA. Licensed CC0.

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