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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85985

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
June 23, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
The Magstim Company Limited

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

Neurosign V4 Intraoperative Nerve monitor family of devices.

Z-2884-2020
Recall number
Z-2884-2020
Initiated
June 23, 2020
Classification
Class II
Status
Terminated
Quantity
49 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Serial numbers # 001 to 049. US product serial number is 039.

Distribution pattern

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.