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