Home / Recalls / Medical Devices
Draeger Medical, Inc. recalls VentStar Watertrap (N) 180, MP00363
Recalled May 24, 2023 · FDA recall Z-1449-2023 · Draeger Medical
Hazard
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces. · FDA Class I
Units
125 units
Sold at
Domestic: US Nationwide Distribution.
Description
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Product
VentStar Watertrap (N) 180, MP00363
Manufacturer(s)
Draeger Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →