Health product recall

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

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

DEFIGARD Touch 7

Lot or serial number
  • 128968000916
  • 128969000990
Model or catalog number

1-128-9900

Companies
Manufacturer

Schiller Medical

4 Rue Louis Pasteur

Wissembourg

67162

FRANCE