Categories
Procedure
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 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
Recall Notice
Merit Recall ID: 1721504-03/11/25-003R
Name of Affected Products: EsophyX® Z+
Action Required: Sign and Return Customer Response Form
Access EsophyX Z+ Device IFU here.
Recall Notice
DIRECT CUSTOMERS OF MERIT
Merit Recall ID: 1721504-05/10/24-005R
Name of Affected Products: Merit Products Containing Plastic Syringes Manufactured by Jiangsu Shenli Medical Production Co Ltd.
Action Required: Device Modification (Over-Label) – Discard Affected Syringes
Merit Medical Systems, Inc. (Merit) is voluntarily conducting a recall of specific lots of Merit products containing plastic syringes manufactured by Jiangsu Shenli Medical Production Co Ltd. (Jiangsu Shenli).
Download Direct Customer Letter
Access the Affected Lots Table here.
PRODUCT DISTRIBUTORS
Name of Affected Products: Merit Products Containing Plastic Syringes Manufactured by Jiangsu Shenli Medical Production Co Ltd.
Action Required: Read and Understand
Merit Medical Systems, Inc. (Merit) is voluntarily issuing this Medical Device Recall Notice pertaining to plastic syringes manufactured by Jiangsu Shenli Medical Production Co Ltd. (Jiangsu Shenli).
Access the Affected Lots Table here.