Magstim recalls Neurosign V4 nerve monitors with serial numbers 001-049 due to potential cable damage from improper handling. Affected units may require repair or replacement.
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.
Magstim is recalling Neurosign V4 intraoperative nerve monitors with serial numbers 001 to :049 because improper cable handling could damage internal components. This could lead to device failure during surgery.
Improper manipulation of the cables connecting the pre-amplifier to the nerve monitor or stimulator pod can damage the internal construction of the cables. This could lead to device failure during surgery if the cables are not properly maintained.
Surgical teams using the Neurosign V4 nerve monitors with serial numbers 001 to 049 in the U.S. are most at risk, as these devices are used during surgery.
Check the serial number on the device, which ranges from 001 to 049 for affected units. The U.S. product serial number is 039.
Look for the serial number on the device, which should be between 001 and 049 for affected units.
Magstim is recalling Neurosign V4 intraoperative nerve monitors with serial numbers 001 to 049 due to potential cable damage from improper handling.
Check the serial number on the device; affected units have serial numbers from 001 to 049 in the U.S., with the specific U.S. product serial number being 039.
The recall record does not specify a remedy, so contact Magstim directly for guidance.
We’ve drafted a message you can send Magstim to request your refund or repair — edit it as you like.
Subject: Recall Z-2884-2020 — Magstim Magstim Hello, I own a Magstim that is covered by recall Z-2884-2020 from Magstim. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
