Product Wiki · Recalls · Health Canada — Medical Devices

Monteris Medical NeuroBlate system (2017-10-05) — recall 57490

Health Canada — Medical Devices · Canada · 2017-11-10 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
57490
Date of alert
2017-11-10
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: After reports of probe damage during four procedures, the investigation concluded a 1.5 MRI system interacted with the NeuroBlate probe such that radiofrequency (rf) energy was transferred to the probe, resulting in unintended heating and damage at the tip of the probe.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/monteris-medical-neuroblate-sy

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