Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating and monitoring cranial motor nerves, especially the facial nerve (VII), during ENT surgical procedures.
FDA Recall Z-0869-2021 · Posted None
Advertisement
Recalling FirmThe Magstim Company Limited
Recall StatusTerminated
Product CodeETN
Date Initiated2020-12-08
Date Terminated2023-02-16
Product Quantity7 units
Reason for Recall
A small number of Neurosign 100 Intraoperative Nerve Monitors may have been dispatched without being configured appropriately for the supply mains within the target Country. The specific deficiency includes:
1. Onboard voltage selector set to 240V (European Standard), versus 120V requirement for the United States and Canada.
2. Fuses installed in the Power Entry Module (PEM) 2xT315mAL (240V Standard), versus the 2xT630mAL requirement for a 120V mains supply.
Firm Action
The firm initiated the recall by email on 12/08/2020. The letter explained the issue, requested the consignee examine the device to confirm that the voltage setting and the fuse ratings are correct.. Should there be a mismatch, the consignee is to discontinue use and notify Magstim Service Department at [email protected] or by telephone +44 (0) 199401241111. The firm will send a service pack for the instrument.
Root Cause
Process control
Distribution Pattern
MN, NC, and NY
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement