FDA Adverse Event Malfunction Summary report: N

DRILL BIT Ø2/1.15 CANN L150/48 3FLUTE

MDR report key: 2924495 · Received January 22, 2013

Report

Report Number
8030965-2013-00192
Event Type
Malfunction
Date Received
January 22, 2013
Date of Event
December 6, 2012
Report Date
December 26, 2012
Manufacturer
SYNTHES GMBH
Product Code
HTW
PMA / PMN Number
K962913
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. DEVICE IS AN INSTRUMENT AND IS NOT IMPLANTED/EXPLANTED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS THE PRODUCT IS ENTERING THE COMPLAINT SYSTEM. THE MANUFACTURING RECORDS WERE REVIEWED AND NO COMPLAINT RELATED ISSUES WERE FOUND.

Additional Manufacturer Narrative · 1

DEVICE USED FOR TREATMENT AND NOT DIAGNOSIS. THE BROKEN SURFACE IS HOMOGENOUS, WHAT INDICATES MATERIAL CONFORMITY AS WELL. THE DRILL BIT IS BROKEN DUE TO MECHANICAL OVERLOADING DURING USE. WE STRONGLY HAVE TO ASSUME THAT THE TIP OF THE DRILL BITS CAME IN STRONG CONTACT WITH THE K WIRE AND BLOCKED WHAT LEAD TO THE BREAKAGE FINALLY. NO PRODUCT FAULT COULD BE DETECTED.

Description of Event or Problem · 1

DEVICE REPORT FROM SYNTHES (B)(4) REPORTS AN EVENT IN (B)(6) AS FOLLOWS: DURING A RADIAL HEAD FRACTURE PROCEDURE USING HCS AND MHS PLATE, TWO DRILL BITS WERE BROKEN. THE SURGEON REMOVED EVERY VISIBLE BROKEN PIECE FROM THE SURGICAL FIELD WITH DIFFICULTY AND THE PROCEDURE WAS COMPLETED USING ANOTHER DRILL BIT. THE SURGEON REPORTEDLY DID FEEL THAT HE PUT EXTRA LOAD ON THE GUIDE WIRE. IT WAS REPORTED THE PATIENT HAD A GOOD BONE QUALITY. THIS IS 2 OF 2 REPORTS FOR THE SAME EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
31327 DRILL BIT Ø2/1.15 CANN L150/48 3FLUTE DRILL BIT HTW SYNTHES GMBH F-10556

Patients

Seq Age Sex Outcome Treatment
1 28 YR DRILL BIT