Bunnell, Inc.

FDA Regulatory Profile

Summary

Total Recalls
2 (1 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0371-2023Class II2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal November 2, 2022
Z-0514-2013Class IPatient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a requirNovember 19, 2012