FDA Recall Terminated

Custom Angiographic Kit

Recall: Z-0621-03 · Initiated February 13, 2003

Recall

Recall Number
Z-0621-03
Event Number
25605
Firm
Merit Medical Systems, Inc
FEI Number
1721504
Product Code
DQO
Status
Terminated
Root Cause
Other
Initiated
February 13, 2003
Posted
March 6, 2003
Terminated
March 7, 2003
Address
1600 West Merit Parkway, South Jordan, UT, 84095

Description

Custom Angiographic Kit

Reason

A recent design change feature in the cap closure design for stopcocks in tubing convenience kits could preclude proper sterilization.

Action

Consignees were notified by phone and FAX on 2/12/2003.

Distribution

FL and Japan.

Quantity

100 kits.