Merit Maestro Microcatheter, 2.4F 130cm Straight, REF28MC24130ST, Rx Only, Non-pyrogenic Sterile if package is unopened or undamaged.
FDA Recall Z-0162-2015 · Posted 2014-10-31
Recalling FirmMerit Medical Systems, Inc.
Recall StatusTerminated
Product CodeKRA
Date Initiated2014-09-26
Date Terminated2014-11-19
Product Quantity56 units
Reason for Recall
These microcatheters were packaged with a 2.8 F distal tip, rather than the labeled 2.4 F.
Firm Action
Consignees were notified via letter on September 26, 2014. Written notification included product identification information, instruction to immediately quarantine any devices and discontinue use, ensure all personnel to whom devices were distributed are made aware of this field action, and instructions to contact their Merit representative. An email notification was sent to US Merit sales representatives with accounts that had received affected product. The affected sales representatives were provided a Customer Response Form applicable to their account, a representative copy of communications sent directly to their affected accounts, and a copy of the Frequently Asked Questions. Merit sales representatives were instructed to visit the account and assist with the return of the affected units back to the Merit Field Assurance Department.
Root Cause
Mixed-up of materials/components
Distribution Pattern
Nationwide and to India. No govt/military/VA consignees.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.