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Health Canada Medical devices

Cardiohelp-I

Issued April 8, 2024
Issue
During service measurements on the Cardiohelp-I devices in the field, it was noticed that the measured patient leakage current exceeded the limit values of 50 μa specified in standard EN 60601-1:2006 + a1:2013. Patient leakage currents of up to 1337 μa were measured. Investigations have shown that only Cardiohelp-I devices with installed sensor panels (701051308) with an old sensor bridge (701049193) hardware version are affected. The new hardware version is not affected. Recall Start Date: March 18, 2024
Hazard description
Performance
Product
Product name
Cardiohelp-I
Reference
ID
RA-75365