Product Wiki · Recalls · Health Canada — Medical Devices

Axiom Sensis System Electrophysiology and Hemodynamic Application… — recall 56963

Health Canada — Medical Devices · Canada · 2017-05-16 · Type II

As described by Health Canada — Medical Devices: Axiom Sensis System Electrophysiology and Hemodynamic Application (2017-04-17)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
56963
Date of alert
2017-05-16
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: In Sensis Systems, a computer that is extremely dusty can cause problems when starting the system. In rare cases, it can cause the Sensis to fail. Should the Sensis System fail, its functions can no longer be used. Clinical treatment may need to be terminated, restarted or transferred to a functioning system.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/axiom-sensis-system-electrophy

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