Product Wiki · Recalls · Health Canada — Medical Devices

ICEfx™ Cryoablation Console — recall 78048

Health Canada — Medical Devices · Canada · 2025-09-11 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
78048
Date of alert
2025-09-11
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Neurology
Product type
Medical devices
Reported risk: Boston Scientific has identified that certain desiccant tube subassemblies, a component of the preventative maintenance (PM) kits used to service ICEfx™ Cryoablation System, were built with end caps that were not correctly tightened. Loose end caps could allow the desiccant to absorb excess atmospheric moisture during storage, potentially impairing argon gas drying and restricting flow due to needle clogging, which could alter therapeutic response. To date Boston Scientific has not received any complaints or reports of patient harm associated with this issue. Recall start date: September 18, 2025
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/icefxtm-cryoablation-console

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