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.
Other Recalls by Baxter Healthcare Corporation
- Class II: Risk 12/22/2025
- Class II: Risk 11/28/2025
- Class II: Risk 10/28/2025
- Class II: Risk 09/17/2025
- Class II: Risk 08/29/2025
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.