Devices

Device Recall Adult AirLife duallimb

Model / Serial
0001100127 0001116871 0001116872 0001124936 0001129065 0001129066 0001129067 0001129069 0001129070 0001131426 0001131428 0001134350 0001135400 0001136027 0001136028 0001136029 0001145151 0001145152 0001145153 0001157125
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
US Nationwide Distribution
Product Description
Adult AirLife dual-limb, dual-heat circuit (Model AH280) with AirLife Humidification Chamber, Model Number AH290. || The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator gasses to patients requiring invasive and non-invasive ventilation.
Manufacturer
Vyaire Medical
1 Event
- Recall of Device Recall Adult AirLife duallimb

Manufacturer

Vyaire Medical

Manufacturer Address
Vyaire Medical, 75 N Fairway Dr, Vernon Hills IL 60061-1845
Manufacturer Parent Company (2017)
Vyaire Holding Company
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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