PlainRecalls
FDA Devices Critical Class I Ongoing

Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP

Reported: January 22, 2025 Initiated: December 20, 2024 #Z-0887-2025

Product Description

Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP

Reason for Recall

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

Details

Units Affected
1 unit
Distribution
US, Nationwide Distribution
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP. Recalled by Baxter Healthcare Corporation. Units affected: 1 unit.
Why was this product recalled?
There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 22, 2025. Severity: Critical. Recall number: Z-0887-2025.