PlainRecalls
FDA Devices Critical Class I Ongoing

Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals

Reported: March 8, 2023 Initiated: January 25, 2023 #Z-1141-2023

Product Description

Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals

Reason for Recall

There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.

Details

Units Affected
8 units
Distribution
Nationwide
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals. Recalled by Baxter Healthcare Corporation. Units affected: 8 units.
Why was this product recalled?
There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 8, 2023. Severity: Critical. Recall number: Z-1141-2023.