Neurosign 100 Nerve Monitor (2020-12-07)

NEUROSIGN 100 Nerve Monitor Recall NeuroSign 100 nerve monitoring devices distributed across Canada are being recalled due to a defect that can cause the device to fail to detect nerve signals during surgery, potentially affecting patient safety during procedures. The devices may not function as intended when monitoring nerve activity. This Class I recall affects all NeuroSign 100 nerve monitors that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-12-31
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ad1c1624-976f-4459-bcbd-744c89952262