FDA Device recall Z-2140-2024
Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0…
- FDA Device
- Class I
- ongoing
- Published 2024-07-03
On 2024-07-03 the FDA classified a Class I recall of Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0… by Baxter Healthcare, citing 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 batter….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2140-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-05-29 |
| Published | 2024-07-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
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.
Reason
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.
Identifiers
| code_info | Life2000 Ventilator: UDI Number: 00887761978089; Product Code: MS-01-0118. Life2000 Ventilator System: a. Product C…Life2000 Ventilator: UDI Number: 00887761978089; Product Code: MS-01-0118. Life2000 Ventilator System: a. Product Code: BT-20-0002; Serial Numbers: 123300001188, 123300001189, 123300001190, 123300001191, 123300001192, 123300001193, 123300001194, 123300001195, 123300001196, 123300001197, 123300001220, 123300001221, 123300001222, 123300001223, 123300001224, 123300001225, 123300001227, 123300001292, 123300001293, 123300001416, 123300001418, 123300001419, 123300001420, 123300001421, 123300001423, 123300001424, 123300001425, 123300001426, 123300001428, 123300001612, 123300001614, 123300001615, 123300001616, 123300001617, 123300001618, 123300001619, 123300001620, 123300001621, 123300001669, 123300001670, 123300001671, 123300001672, 123300001673, 123300001674, 123300001675, 123300001676, 123300001677, 123300001678, 123300001683, 123300001684, 123300001685, 123300001688, 123300001689, 123300001690, 123300001691, 123300001769, 123300001770, 123300001771, 123300001772, 123300001773, 12330000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2140-2024%22
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