FDAFDA · Food and drugs·Recall number Z-3262-2024
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.
Published October 2, 2024 · Recall initiated: August 7, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Fisher & Paykel Healthcare, Ltd.
- Distributor
- 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
- Lot
- Model Number: PT301US UDI-DI code: 09420012466662 Lot/Serial Numbers:
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- New Zealand
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