The Magstim Company Limited: Medical Device Recall in 2020 - (Recall #: Z-2884-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Neurosign V4 Intraoperative Nerve monitor family of devices.

Product Classification:

Class II

Date Initiated: June 23, 2020

Date Posted: September 2, 2020

Recall Number: Z-2884-2020

Event ID: 85985

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.

Status: Terminated

Product Quantity: 49 devices

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.

Voluntary or Mandated:

Voluntary: Firm initiated