FDA Adverse Event Malfunction Summary report: N

LCP PROXTIBPL 3.5 LAT R SHAFT 4HO L81 TI

MDR report key: 2831450 · Received October 11, 2012

Report

Report Number
3003506883-2012-00314
Event Type
Malfunction
Date Received
October 11, 2012
Report Date
September 12, 2012
Manufacturer
SYNTHES (USA)
Product Code
HRS
PMA / PMN Number
K030597
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE RAW MATERIAL AND DEVICE HISTORY RECORDS WERE REVIEWED AND NOTHING WAS FOUND THAT WOULD CAUSE OR CONTRIBUTE TO THE REPORTED CONDITION.

Additional Manufacturer Narrative · 1

THIS DEVICE IS USED FOR TREATMENT NOT DIAGNOSIS. THE INVESTIGATION FOUND THAT THE THREAD HOLES OF THE LCP PLATE CAN CUT THE USPU THREADS.

Additional Manufacturer Narrative · 1

THIS DEVICE IS USED FOR TREATMENT, NOT DIAGNOSIS. THE AS RECEIVED CONDITION OF THE PLATE IS THAT THE SURFACE ANODIZE IS SLIGHTLY DISCOLORED FROM GOLD TO PINK CONSISTENT WITH NORMAL HANDLING. THERE ARE SOME SCRATCHES TO THE ANODIZED SURFACE IN THE NECK AREA OF THE PLATE AND ON THE TOP AND BOTTOM SURFACE OF THE HEAD. ALL THREADED AND NON-THREADED HOLES HAVE THE NORMAL ANODIZED SURFACE FINISH WITH NO DAMAGE EVIDENT.

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT. THE MANUFACTURING REPORT NUMBER WAS CORRECTED FROM "3003506883-2012-0314" TO "3003506883-2012-00314."

Description of Event or Problem · 1

A DEVICE REPORT FROM (B)(6) INDICATED A HOSPITAL REPORTED: A RESPONSIBLE PERSON OF THE HOSPITAL FOUND THAT THREADS ON THE PLATE HOLES TEAR OFF/ STRIPPED WHEN TIGHTENING. AFTER PERVADING OF THE FIBERS THROUGH THE PROXIMAL THREAD HOLES, THE FIBERS TEAR OFF WHEN TIGHTENING. THERE WAS NO PT INVOLVEMENT. THIS IS 9 OF 13 REPORTS FOR THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LCP PROXTIBPL 3.5 LAT R SHAFT 4HO L81 TI LCP PROXTIBPLATE HRS SYNTHES (USA) 6407403

Patients

Seq Age Sex Outcome Treatment
1