FDA Adverse Event Injury Summary report: N

NAIL,FIXATION,BONE

MDR report key: 5803445 · Received July 19, 2016

Report

Report Number
2520274-2016-13517
Event Type
Injury
Date Received
July 19, 2016
Report Date
July 7, 2016
Manufacturer
SYNTHES USA
Product Code
JDS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. MEHBOOB, I (2009). PROXIMAL FEMORAL NAIL IN INTERTROCHANTERIC FEMORAL FRACTURES. J NEPAL MED ASSOC, 48, 273-275. THIS REPORT IS FOR UNKNOWN PROXIMAL FEMORAL NAIL (PFN) SYSTEM/UNKNOWN QUANTITY/UNKNOWN LOT. (B)(4). THE INVESTIGATION COULD NOT BE COMPLETED AND NO CONCLUSION COULD BE DRAWN, AS NO DEVICE WAS RETURNED AND NO LOT NUMBER OR PART NUMBER WAS PROVIDED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. (B)(4).

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING LITERATURE ARTICLE MEHBOOB, I (2009). PROXIMAL FEMORAL NAIL IN INTERTROCHANTERIC FEMORAL FRACTURES. J NEPAL MED ASSOC, 48, 273-275. PAKISTAN. A RETROSPECTIVE MULTICENTERED STUDY WAS CONDUCTED DONE AT TWO INSTITUTIONS, POSTGRADUATE MEDICAL INSTITUTE, LAHORE AND SINDH GOVERNMENT LYARI GENERAL HOSPITAL, KARACHI FROM FEBRUARY, 2005 - FEBRUARY, 2007 FOR UNSTABLE FRACTURES OF PROXIMAL FEMUR USING THE PROXIMAL FEMORAL NAIL. TWENTY-SIX CASES OPERATED DURING TWO YEARS OF STUDY WHICH HAD COMPLETED AT LEAST A YEAR OF FOLLOW UP. ALL HAD BEEN TREATED USING A PROXIMAL FEMORAL NAIL FOR UNSTABLE INTERTROCHANTERIC FRACTURES OF FEMUR. A RADIOLOGICAL ASSESSMENT WAS MADE WITH SERIAL X-RAYS. THE AVERAGE AGE OF THE STUDY POPULATION WAS 57.24 YEARS (RANGE: 35-70 YEARS). TOTAL 10/26 WERE INJURED IN A ROAD TRAFFIC ACCIDENT AND REST HAD DOMESTIC FALL. COMPLICATIONS: THIS REPORT IS FOR AN UNKNOWN PROXIMAL FEMORAL NAIL (PFN) SYSTEM. ONE PATIENT COMPLAINED OF PAIN OVER THE TROCHANTER AREA DURING FOLLOW UP. TWO PATIENTS EXPERIENCED SHORTENING. THIS IS REPORT 2 OF 2 FOR (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
456392 NAIL,FIXATION,BONE JDS SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention