FDA Recall
Terminated
Fluid Management Set. Catalog Number K08-MP5159A
Recall: Z-0631-2017
·
Initiated September 23, 2016
Recall
- Recall Number
- Z-0631-2017
- Event Number
- 75367
- Firm
- Merit Medical Systems, Inc.
- FEI Number
- 1721504
- Product Code
- OJV
- Status
- Terminated
- Root Cause
- Process control
- Initiated
- September 23, 2016
- Posted
- November 19, 2016
- Terminated
- March 27, 2017
- Address
- 1600 W Merit Pkwy South, Jordan, UT, 84095-2416
Description
Fluid Management Set. Catalog Number K08-MP5159A
Reason
Merit Medical Systems, Inc. announces a voluntary field action for various Merit Medical Procedure Kits due to a compromised sterile barrier.
Action
Consignees notified via letter on 09/23/16 to quarantine any devices and discontinue use, ensure all personnel to whom the devices were distributed are made aware of the field action, and return affected devices to Merit Medical.
Distribution
Nationwide to VA, UT, and NC. Other foreign consignee Japan. No Canadian and VA/govt/military consignees.
Quantity
178 units