# FDA recall Z-0742-2022

> **bioMerieux, Inc.** · Class II · device recall initiated 2022-02-09.

## Product

VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.

## Reason for recall

Invalid calibrations (out of range high) while using the product.

## Distribution

Distribution was made to CA, FL, GA, IL, IN, LA, MA, MD, ME, MO, NJ, NY, OH, PA, TX, VA, WI, and WV.  There was government distribution but no military or foreign distribution.

## Key facts

- **Recall number:** Z-0742-2022
- **Recalling firm:** bioMerieux, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-09
- **Report date:** 2022-10-05
- **Termination date:** 2026-04-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Durham, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0742-2022

## Citation

> AI Analytics. FDA recall Z-0742-2022. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0742-2022. Source: US FDA. Licensed CC0.

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