PlainRecalls
FDA Devices Critical Class I Terminated

Ventstar Coax 180, MP03374

Reported: May 24, 2023 Initiated: April 17, 2023 #Z-1455-2023

Product Description

Ventstar Coax 180, MP03374

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
18,160 units
Distribution
Domestic: US Nationwide Distribution.
Location
Telford, PA

Frequently Asked Questions

What product was recalled?
Ventstar Coax 180, MP03374. Recalled by Draeger Medical, Inc.. Units affected: 18,160 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-1455-2023.