Official recall record
Servo-N
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-02-02
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
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.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.