Health product recall

FRED Easyport

Brand(s)
Last updated

Summary

Product
FRED Easyport
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Industry

Affected products

Affected products Lot or serial number Model or catalog number
FRED Easyport All lots. 0.900000

Issue

Schiller Ag has become aware of instances of the FRED Easyport failing the maintenance caused by defective IGBT modules. Failure of the IGBT module may result in the device only being able to deliver a limited number of shocks.

Recall Start Date: April 1, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Schiller Ag

Altgasse 68, Baar, Zug, Switzerland, 6341

Published by
Health Canada
Audience
Industry
Recall class
Type II
Identification number
RA-77313

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