FDA Enforcement Class II Terminated

KimVent* Closed Suction System for Adults, 14 F, DSE, DT (Product Code 22109) A tracheobronchial suction catheter is a device that is attached to a port of the airway circuit for use as needed to aspirate liquids or semisolids from a patient's upper airway.

Recall: Z-2509-2015 · Reported September 9, 2015

Enforcement

Recall Number
Z-2509-2015
Event ID
71966
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Halyard Health, Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
September 9, 2015
Initiation Date
July 29, 2015
Classification Date
August 31, 2015
Termination Date
January 12, 2016
Address
5405 Windward Pkwy, N/A, Alpharetta, GA, 30004-3894, United States

Description

KimVent* Closed Suction System for Adults, 14 F, DSE, DT (Product Code 22109) A tracheobronchial suction catheter is a device that is attached to a port of the airway circuit for use as needed to aspirate liquids or semisolids from a patient's upper airway.

Reason

The thumb valve of some KIMVENT Closed Suction Systems remained partially open after suctioning was completed, even though the valve appeared to be closed or in the "LOCKED" position.

Code Info

Product Code 22109 - M5082T607

Distribution

Worldwide Distribution - US (nationwide and Puerto Rico and Internationally to Canada

Quantity

N/A