Health product recall

Servo-N

Last updated

Summary

Product
Servo-N
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 catalog number

Servo-N

v. 4.4 or 4.5 with HFO-option

6688600

Issue

A limitation of the intended performance of Servo-N during high frequency oscillatory ventilation (HFOV) when using the Fisher & Paykel Neonatal Circuit (950N81*) and the humidifier FP950. The use of a relatively small endotracheal (ET) tube in relation to body weight and in combination with the Fisher & Paykel Neonatal Circuit* that is used with the FP950 humidifier limits the delivered Pampl and therefore reduces the delivered VThf.

Recall Start Date: January 22, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies

Maquet Critical Care Ab

Rontgenvagen 2, Solna, Sweden, 17154

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74999

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