Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.
Reason for recall: Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier. Distribution: US Nationwide distribution and Puerto Rico. No international distribution. Quantity: 129 units Lot/code info: Model Number: 6888800. UDI-DI: 07325710010518. All software versions.
07325710010518
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.