Quick summary
Quick summary: Defigard Touch7.
Public recall detail
Defigard Touch7
Recall
Safety notice
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Defigard Touch7.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandSchiller Medical
ProductDefigard Touch7
IssueMedical devices - Performance
Recall classType II
IdentificationRA-64314
Affected products
ProductDefigard Touch7
Lot128968000814 128960002876 128968000916 128960002954 128967000108 128960002953 128969000990
Model1-128-9900
Serial number128968000814 128960002876 128968000916 128960002954 128967000108 128960002953 128969000990
DescriptionDefigard Touch7
Issue
In rare cases, when the device is switched on directly in defibrillator mode, cancellations of heart rhythm analysis after 30 seconds have been reported. Recall start date: June 17, 2022
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceIndustry
CategoryHealth products - Medical devices - Cardiovascular
CompaniesSchiller Medical 4 Rue Louis Pasteur, Wissembourg, France, 67160
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64314
Background{}
CompaniesSchiller Medical 4 Rue Louis Pasteur, Wissembourg, France, 67160
AudiencesIndustry
Source updated2022-06-27
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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