# FDA recall Z-0024-2020

> **Stryker Instruments Div. of Stryker Corporation** · Class II · device recall initiated 2019-07-31.

## Product

C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 07613327277319    Product Usage:  The C2 Nerve Monitor System is intended for intra-operative monitoring and stimulation for localization and identification of cranial and peripheral motor and mixed motor sensory nerves during surgery.

## Reason for recall

Stryker C2 NerveMonitor's design and instructions may not optimally address usability issues related to  the functionality of the device, which may result in use errors potentially causing or contributing to nerve  injury.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0024-2020
- **Recalling firm:** Stryker Instruments Div. of Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-31
- **Report date:** 2019-10-09
- **Termination date:** 2021-03-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0024-2020

## Citation

> AI Analytics. FDA recall Z-0024-2020. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-0024-2020. Source: US FDA. Licensed CC0.

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