Baxter Healthcare Corporation: Device Recall

Recall #Z-2140-2024 · 05/29/2024

Class I: Dangerous

Recall Details

Recall Number
Z-2140-2024
Classification
Class I
Product Type
Device
Recalling Firm
Baxter Healthcare Corporation
Status
Ongoing
Date Initiated
05/29/2024
Location
Deerfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2,510 units

Reason for Recall

Potential for certain Life2000 ventilator systems to either fail to charge or have intermittent charging behavior due to damage to the battery charger dongle. Damage of the battery charger dongle prevents the ventilator's internal battery from charging.

Product Description

Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.

Distribution Pattern

US Nationwide distribution.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.