Bunnell Recalls
2 recalls on record · December 26, 2012 to December 14, 2022 · Medical Devices
Recalls by year
12
22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 14, 2022Medical DevicesFDA
Bunnell, Inc. recalls 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside
Hazard: Some adaptors, for use with high frequency ventilators, were packaged improperly, and may deform at the tip, which may impair the ability to pass a suction catheter or may affect normal ventilator performance, which may lead to hypercarbia, hypoxia, and gas trapping.
December 26, 2012Medical DevicesFDA
Bunnell, Inc. recalls Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a required disposable compon
Hazard: Customer complaints received indicate the heater wire insulation can melt, causing a short which creates sparking and smoke, in the circuit close to the humidifier cartridge. Bunnell is recalling all lots of circuits distributed between March 12, 2012 and November 30, 2012.