Product Notices

Recall Notice

Merit Recall ID: 1721504-10/05/26-009R
Name of Affected Products: Workstation Sheath: Surfacer® Inside-Out® Access Catheter System
Action Required: Destroy at point of use

Please review customer letter and review inventory, if you are in possession of any of affected product please contact RESPONSE@merit.com.

Recall Notice

Merit Recall ID: 1721504-08/26/26-008R
Name of Affected Products: Merit Embosphere^® Microspheres (Korea)
Action Required: Return product to Merit

Download Customer Letter (KOR)

Recall Notice

Merit Recall ID: 1721504-08/26/26-007R
Name of Affected Products: SCOUT MD™ Delivery System
Action Required: Return product to Merit

Download Customer Letter (EN)

Recall Notice

Merit Recall ID: 1721504-07/16/26-006R
Name of Affected Products: Merit Embosphere^® Microspheres
Action Required: Return product to Merit

Download Customer Letter (US / CAN)

Recall Notice

Merit Recall ID: 1721504-11/25/25-008R
Name of Affected Products: basixCOMPAK™ Inflation Device
Action Required: Read and Understand; Sign and Return Customer Response Form

Download Customer Letter (EN)

Download EU Field Safety Notice (EN)

Note: Additional languages may be available upon request

Recall Notice

Merit Recall ID: 1721504-07/29/25-007R
Name of Affected Products: PhD Hemostasis Valve™
Action Required: Return Product to Merit, Sign and Return Customer Response Form

Download Customer Letter (EN)

Recall Notice

Merit Recall ID: 1721504-03/11/25-003R
Name of Affected Products: EsophyX^® Z+
Action Required: Sign and Return Customer Response Form

Download Customer Letter

Access EsophyX Z+ Device IFU here.