FDA Device recall Z-2884-2020
Neurosign V4 Intraoperative Nerve monitor family of devices
- FDA Device
- Class II
- terminated
- Published 2020-09-02
On 2020-09-02 the FDA classified a Class II recall of Neurosign V4 Intraoperative Nerve monitor family of devices by The Magstim, citing 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 damag….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2884-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-23 |
| Published | 2020-09-02 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | The Magstim |
| Distribution | MN |
Product
Neurosign V4 Intraoperative Nerve monitor family of devices.
Reason
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.
Identifiers
| code_info | Serial numbers # 001 to 049. US product serial number is 039. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2884-2020%22
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