FDA Adverse Event Malfunction Summary report: N

CONTOURED CROSSBAR LARGE 5.5 ROD

MDR report key: 4144173 · Received April 28, 2014

Report

Report Number
2032593-2014-00021
Event Type
Malfunction
Date Received
April 28, 2014
Date of Event
March 28, 2014
Report Date
April 3, 2014
Manufacturer
SEASPINE, INC.
Product Code
KWP
PMA / PMN Number
K072605
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE INVOLVED IN THE REPORTED INCIDENT HAS BEEN RECEIVED FOR EVALUATION. AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFORMATION.

Description of Event or Problem · 1

THIS IS THE FIRST REPORT OF TWO REPORTS CONCERNING THE SAME PATIENT SURGERY. THIS REPORT CONCERNS THE MALIBU CONTOURED CROSSBAR LARGE 5.5 ROD (PRODUCT ID 12-2075). IT WAS REPORTED DURING A L5-S1 ANTERIOR-POSTERIOR FUSION SURGERY, A MALIBU LARGE CROSSBAR (12-2075) BROKE WHILE BEING TIGHTENED WITH A TORQUE LIMITING SCREWDRIVER. THE SCREWS (TWO) THAT ATTACH THE CROSSBAR TO THE ROD WERE TIGHTENED FIRST. DURING TIGHTENING OF THE MIDDLE SCREW (THAT ADJUSTS THE LENGTH OF THE CROSSBAR) THE SCREW WS SHEARED FROM THE CROSSBAR ASSEMBLY. THE SURGEON REMOVED THE CROSSBAR AND REPLACED IT WITH ANOTHER ONE OF THE SAME SIZE WITHOUT INCIDENT. THE PATIENT WAS NOT HARMED AND THE SURGERY WAS DELAYED BY APPROXIMATELY TWO MINUTES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
253982 CONTOURED CROSSBAR LARGE 5.5 ROD MALIBUE KWP SEASPINE, INC. M12593C

Patients

Seq Age Sex Outcome Treatment
1