FDA recall Z-0488-2024

Vyaire Medical · Class II · device

Product

vyaire Flexible Patient Circuit, 3100A, REF 29028-003, intended to be used with the 3100A High Frequency Oscillatory Ventilator (HFOV)

Reason for recall

Two patient circuits, 29028-003 and 29028-004, for the 3100 High Frequency Oscillatory ventilator that are only approved for use outside the U.S. were distributed in the U.S.

Distribution

US: Florida

Key facts

Status
Completed
Initiation date
2023-10-27
Report date
2023-12-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mettawa, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0488-2024