DEFIGARD Touch 7 (2019-08-13)

Starting date:

August 13, 2019

Posting date:

September 25, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-73979

Last updated:
2020-09-25

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  Reason
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  Affected products

Affected Products

DEFIGARD Touch 7

Reason

When the device fails to transmit the interventions during months (GSM network problem, ...) accumulations of temporary files that causes the inability of the device to switch to automated external defibrillation mode (AED).

Affected products