ProductGuru Recalls

Official recall record

FRED Easyport

Health Canada — Medical Devices · 2025-04-22 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-04-22
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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