Neurosign V4 Intraoperative Nerve monitor family of devices — Class II medical device recall Z-2884-2020
Terminated recall by The Magstim Company Limited, reported 2020-09-02, distributed in MN. Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable wh
| Recall number | Z-2884-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Magstim Company Limited, Whitland, N/A, United Kingdom |
| Recall initiated | 2020-06-23 |
| Classified | 2020-08-25 |
| Reported by FDA | 2020-09-02 |
| Terminated | 2024-08-16 |
| Distributed | MN |
| Countries outside the US | BE, BR, CA, CL, ES, GB, GR, IE, NL, NZ, PK, PL, PT, TH |
| Quantity | 49 devices |
| Serial numbers | 001, 039, 049 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2884-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.