FDA Adverse Event Malfunction Summary report: N

GMK FEMORAL CUTTING GUIDE

MDR report key: 2111031 · Received April 13, 2011

Report

Report Number
3005180920-2011-00018
Event Type
Malfunction
Date Received
April 13, 2011
Date of Event
March 16, 2011
Report Date
April 13, 2011
Manufacturer
MEDACTA INTERNATIONAL SA
Product Code
JWH
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

A DOCUMENT REVIEW OF THE LOT 096776 ((B)(4)) WAS DONE AND NO ANOMALIES WERE FOUND RELATED TO THE PROBLEM OCCURRED. NO OTHER SIMILAR EVENT WAS REPORTED CONCERNING THIS LOT. THE BREAKAGE IS THOUGHT TO BE ASSOCIATED TO AN IMPROPER USE DURING PREVIOUS SURGERIES: IN ORDER TO ASSURE A CLOSE CONTACT BETWEEN THE CUTTING GUIDE AND THE DISTAL CUT, HAMMER HITS WERE PROBABLY DONE BY THE SURGEON AND THESE HAVE PROGRESSIVELY WEAKENED THE PIECE LEADING TO ITS BREAKAGE. ON THE BASIS OF MEDACTA'S RISK ANALYSIS, THE FAILURE MODE IS HIGH UNLIKELY TO CAUSE PT HARM SINCE, ALSO IN CASE OF BREAKAGE, THE CUTS COULD BE PERFORMED BECAUSE THE GUIDE IS FIXED TO THE BONE WITH THE PINS, AS HAPPENED IN THIS CASE. THIRTEEN SIMILAR EVENTS WERE REPORTED TO FDA: 2010-00035; 2010-00040; 2010-00041; 2010-00042; 2010-00046; 2010-00047; 2011-00004; 2011-00005; 2011-00006; 2011-00010; 2011-00014; 2011-00016; 2011-00017 AND A FOLLOW-UP TO EXPLAIN THE MODIFICATION/ADJUSTMENT DECIDED, WAS ALREADY SENT ON (B)(4) 2011. THE FOLLOW-UP IS APPLICABLE ALSO TO THIS EVENT.

Description of Event or Problem · 1

THE CUTTING GUIDE BROKE IN TWO PIECES DURING IMPACTION. NO PT/USER HARM. THE SURGERY WAS COMPLETED SUCCESSFULLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GMK FEMORAL CUTTING GUIDE REUSABLE SURGICAL INSTRUMENT FOR KNEE JWH MEDACTA INTERNATIONAL SA 096776

Patients

Seq Age Sex Outcome Treatment
1 UNK