PlainRecalls
FDA Devices Critical Class I Terminated

VentStar Watertrap (N) 180, MP00363

Reported: May 24, 2023 Initiated: April 17, 2023 #Z-1449-2023

Product Description

VentStar Watertrap (N) 180, MP00363

Reason for Recall

Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

Details

Recalling Firm
Draeger Medical, Inc.
Units Affected
125 units
Distribution
Domestic: US Nationwide Distribution.
Location
Telford, PA

Frequently Asked Questions

What product was recalled?
VentStar Watertrap (N) 180, MP00363. Recalled by Draeger Medical, Inc.. Units affected: 125 units.
Why was this product recalled?
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 24, 2023. Severity: Critical. Recall number: Z-1449-2023.