# FDA recall Z-2884-2020

> **The Magstim Company Limited** · Class II · device recall initiated 2020-06-23.

## Product

Neurosign V4 Intraoperative Nerve monitor family of devices.

## Reason for recall

Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connects the pre-amplifier to the stimulator pod, may cause damage to the internal construction of the cables.

## Distribution

Domestic: MN  International: UK, Republic of Ireland, Spain, Netherlands, Canada. (Technomed Europe distributed to: Brazil, Spain, Belgium, Chile, Greece, Poland, New Zealand, Pakistan, Portugal and Thailand.

## Key facts

- **Recall number:** Z-2884-2020
- **Recalling firm:** The Magstim Company Limited
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-23
- **Report date:** 2020-09-02
- **Termination date:** 2024-08-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Whitland, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2884-2020

## Citation

> AI Analytics. FDA recall Z-2884-2020. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2884-2020. Source: US FDA. Licensed CC0.

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