Health product recall

Nim Trivantage Emg Endotracheal Tube

Last updated

Summary

Product
Nim Trivantage Emg Endotracheal Tube
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Nim Trivantage Emg Endotracheal Tube

More than 10 numbers, contact manufacturer.

8229707

Nim Trivantage Emg Endotracheal Tube 3pk

More than 10 numbers, contact manufacturer.

8229737

Issue

Medtronic has received 87 complaints as of October 5th, 2023 indicating potential health hazards of degraded or loss of functionality of the device with specific lots. The potential hazards can cause unintended extubation, a delay or a cancelation of the case or dysphonia, dysphagia, dyspnea, or possible nerve damage.

Recall start date: November 7, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies
Medtronic Xomed Inc.
6743 Southpoint Drive North, Jacksonville, Florida, United States, 32216
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74661

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