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Recall Observatory FDA recall evidence

Device product

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.

Z-3262-2024

August 07, 2024

Class II

Product summary

Firm
Fisher & Paykel Healthcare, Ltd.
Event
Event 95173
Status
Ongoing
Classification
Class II
Quantity
944 units
Official record key
device-enforcement:Z-3262-2024

Official wording

Reason: Due to a software issue, affected devices that are set up with High Pressure Oxygen (HPO), if the flow alignment alarm occurs, the device will deliver room air only. If this happens, a patient my experience oxygen desaturation that could lead to hypoxia.

Code information: Model Number: PT301US UDI-DI code: 09420012466662 Lot/Serial Numbers:

Distribution pattern: U.S.: AZ, CA, CO, CT, DC, FL, GA, IA, IL, KY, MA, MD, MI, MN, MO, MT, ND, NH, NJ, NV, NY, OH, OR, PA, SD, TX, UT, VA and WA. O.U.S.: Not provided

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software issue