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

Recall Z-1141-2023 — Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals

U.S. FDA — Device Enforcement · United States · 2023-01-25 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1141-2023
Date of alert
2023-01-25
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: There is the potential for patient desaturation events to occur under certain scenarios when the Life2000 ventilation system is connected with an oxygen concentrator.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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