RecallRadar

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…

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

AgencyFDA Device
Recall numberZ-2140-2024
ClassificationClass I
Statusongoing
Initiated2024-05-29
Published2024-07-03
Last updated2026-09-13 11:57 UTC
CompanyBaxter Healthcare
DistributionUS

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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.