CanadaEndoflip System catheters (EF and ES) used with EF-100/DLEF-100 systems, model/catalogue numbers EF-100 or DLEF-100, all lots/serial numbers, are affected. Catheters used after 1‑January‑2026 will be incorrectly flagged as expired due to the system’s 24‑hour usage limit, rendering the catheter unavailable for clinical procedures. Contact the manufacturer if you require additional information.
What's being recalled
Companies: Covidien LLC, 15 Hampshire Street, Mansfield, Massachusetts, United States, 02048.
How to identify it
Affected products: Endoflip System; Lot or serial number: All lots.; Model or catalogue number: DLEF-100
Affected products: Endoflip System; Lot or serial number: All lots.; Model or catalogue number: EF-100
The hazard
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
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States