PlainRecalls
FDA Devices Moderate Class II Terminated

VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.

Reported: March 17, 2021 Initiated: January 29, 2021 #Z-1179-2021

Product Description

VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.

Reason for Recall

Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient.

Details

Recalling Firm
Draeger Medical, Inc.
Units Affected
150 units
Distribution
US Nationwide distribution.
Location
Telford, PA

Frequently Asked Questions

What product was recalled?
VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP00363 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.. Recalled by Draeger Medical, Inc.. Units affected: 150 units.
Why was this product recalled?
Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 17, 2021. Severity: Moderate. Recall number: Z-1179-2021.