Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by Halyard Health, Inc Due to The thumb valve of some KIMVENT Closed Suction...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Halyard Health, Inc directly.
Affected Products
KimVent* Multi-Access Port Replacement Catheter for Adults,Tracheostomy, 14 F (Product Code 2401453-5) 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.
Quantity: N/A
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Halyard Health, Inc
Halyard Health, Inc has 48 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report