ProductGuru Recalls

Official recall record

Neonatal-Infant and Adult Pediatric Filter and Sampling Lines

Health Canada — Medical Devices · 2025-03-06 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-03-06
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Medtronic is issuing an update to Instruction For Use (IFU) following reports of difficulty or inability in disconnecting the adapter from patient's endotracheal tube to perform a procedure. As noted in the IFU, during setup, ensure that the airway adapter can be easily attached and detached from the breathing circuit/tubing before proceeding. Recall Start Date: February 19, 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.

More recalls: Health Canada — Medical Devices · Canada · all filters

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