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Nim trivantage emg endotracheal tube
Official notice
28 Nov 2023
Last checked
28 Nov 2023
An official Health Canada notice concerns Nim trivantage emg endotracheal tube. 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 Published 2023-11-28.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74661
Official notice
2023-11-28
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Medtronic Xomed, Nim Trivantage Emg Endotracheal Tube.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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