Fisher & Paykel Healthcare, Ltd.: Medical Device Recalls in 2024

According to to data from the FDA, there were 2 medical device recalls made by Fisher & Paykel Healthcare, Ltd. in 2024. See the details of the recalls below.

You can see similar recalls for other firms.

• PT301US Airvo 3 Respiratory Support Device with software version 1.2.0 and/or 1.5.1 The Airvo 3 is intended to provide high flow warmed and humidified respiratory gases for administration to spontaneously breathing infant, child, adolescent and adult patients in hospitals and sub-acute facilities.
• Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US