FDA recall Z-0158-2026

Fisher & Paykel Healthcare, Ltd. · Class II · device

Product

Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723

Reason for recall

When unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound audible alert for less than 120 seconds, which may delay user awareness to reconnect power, which could lead to oxygen desaturation, hypoxia. Disinfection kit user manual updated to include checking the audible alert prior to use on a new patient.

Distribution

US Nationwide distribution including in the states of TX, MS, LA, NC, TN, NY, FL, IL, UT, MT, OH, MI, NJ, AR, GA, WI, CA, IN, OK, CO, AL, SC, AZ, MD, WA, MO, PA, MA, NH, KY, KS, VA, CT, MN, ND, NM, NE, IA, WV, ID, NV, OR, HI, VT, RI, AL, SD, WY, PR, ME.

Key facts

Status
Ongoing
Initiation date
2025-09-18
Report date
2025-10-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Auckland, New Zealand

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0158-2026