FDA Adverse Event Malfunction Summary report: N

MESHGRAFT II COMPLETE

MDR report key: 2772229 · Received October 2, 2012

Report

Report Number
1526350-2012-00240
Event Type
Malfunction
Date Received
October 2, 2012
Date of Event
August 20, 2012
Report Date
September 5, 2012
Manufacturer
ZIMMER SURGICAL
Product Code
FZW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE WAS RETURNED TO THE MANUFACTURER FOR REPAIR AND EVALUATION. THE SERVICE RECORD INDICATES THAT THE DEVICE IS 2 YEARS OLD AND WAS LAST RETURNED TO THE MANUFACTURER FOR REPAIR ON (B)(4) 2010. INSPECTION OF THE DEVICE IDENTIFIED A MISSING SET SCREW IN THE RATCHET AND A VERY SMALL DING IN THE CUTTER. THE DEVICE PRODUCED AN ACCEPTABLE TEST MESH. HOWEVER, THE CUTTER WAS REPLACED DUE TO BEING DAMAGED AND DULL. A DULL CUTTER COULD HAVE CAUSED THE CUSTOMER'S EVENT. THE CAUSE IS MOST LIKELY DUE TO THE USER NOT MAINTAINING THE DEVICE PER PREVENTIVE MAINTENANCE AND HANDLING ACCORDING TO THE INSTRUCTIONS FOR USE. THE MESHGRAFT II TISSUE EXPANSION SYSTEM SHOULD BE RETURNED EVERY 12 MONTHS FOR INSPECTION AND PREVENTIVE MAINTENANCE. ANNUAL FACTORY CALIBRATION CHECKS ARE STRONGLY RECOMMENDED TO VERIFY CONTINUED ACCURACY. THE DEVICE WAS SERVICED AND RETURNED TO THE CUSTOMER.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE ZIMMER MESHGRAFT II WAS NOT CUTTING CORRECTLY. ADDITIONAL CLINICAL FOLLOW UP WITH THE HOSPITAL INDICATED THAT THE GRAFT WAS CHEWED UP AND WAS NOT MESHED. THE SURGEON MANUALLY PERFORATED THE INITIAL GRAFT TISSUE FOR USE; HOWEVER, THIS WAS INDICATED TO HAVE INCREASED THE PLANNED SURGICAL TIME BY THIRTY MINUTES. THERE WAS NO REPORT OF AN ADDITIONAL DONOR HARVEST OR MEDICAL INTERVENTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MESHGRAFT II COMPLETE MESHGRAFT II COMPLETE FZW ZIMMER SURGICAL NA NA

Patients

Seq Age Sex Outcome Treatment
1