ProductGuru Recalls

Official recall record

Endoflip System

Health Canada — Medical Devices · 2026-05-14 · CanadaType I
Issuing authority
Health Canada — Medical Devices
Published
2026-05-14
Country of alert
Canada
Alert level
Type I
Alert type
recall

What the authority reported

The issue concerns a problem affecting EF and ES catheters used with EF-100 systems after 1-January-2026. Following this date will be incorrectly flagged as expired due to the system's 24-hour usage limit, rendering the catheter unavailable for clinical procedures.

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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