Product Wiki · Recalls · U.S. FDA — Device Enforcement

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-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.

U.S. FDA — Device Enforcement · United States · 2024-05-29 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2140-2024
Date of alert
2024-05-29
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00887761978089
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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