FDA Adverse Event Injury Summary report: N

NAIL, FIXATION, BONE

MDR report key: 3709514 · Received March 28, 2014

Report

Report Number
2520274-2014-10514
Event Type
Injury
Date Received
March 28, 2014
Date of Event
July 28, 2013
Report Date
March 18, 2014
Manufacturer
SYNTHES (USA)
Product Code
JDS
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. ADDITIONAL NARRATIVE: THIS REPORT IS FOR UTN NAIL 8MM, UNKNOWN PART/UNKNOWN LOT. WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED. SALEM, KHALED (2013, JUL 28): UNREAMED INTRAMEDULLARY NAILING IN DISTAL TIBIAL FRACTURES; INTERNATIONAL ORTHOPAEDICS (SICOT) (2013)37:2009-2015. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING JOURNAL ARTICLE : "UNREAMED INTRAMEDULLARY NAILING IN DISTAL TIBIAL FRACTURES; KHALED HAMED SALEM; INTERNATIONAL ORTHOPAEDICS (SICOT) (2013)37:2009-2015 THE STUDY INCLUDED 101 DISPLACED UNSTABLE FRACTURES OF THE DISTAL TIBIAL THIRD TREATED USING UNREAMED NAILING. THERE WERE 66 MEN AND 35 WOMEN WITH A MEAN AGE OF 39.9 YEARS. UNION OCCURRED AFTER A MEAN TIME OF 23.9 WEEKS. THERE WERE 13 CASES OF DELAYED UNION AND SEVEN NON-UNIONS; ALL HEALED EVENTUALLY WITH ADDITIONAL SURGERY IN ONLY SIX FRACTURES. OF THE SEVEN NON-UNION CASES, 1 WAS A FEMALE PATIENT. MALUNION WAS SEEN IN 12 CASES, TEN OF WHICH WERE ASSOCIATED WITH UNPLATED FIBULAR FRACTURES. THREE FRACTURES (TWO OPEN) WERE TREATED FOR DEEP INFECTION, TWO OF THESE PATIENTS HAD SEPTIC NAIL LOOSENING AND BACKED-OUT DISTAL LOCKING SCREWS. THE MOST COMMON COMPLICATION SEEN WAS FATIGUE FAILURE OF THE LOCKING SCREWS. POSTOPERATIVE BREAKAGE WAS ALSO REPORTED WITH THE LOCKING SCREWS. BROKEN LOCKING SCREWS WERE REMOVED AT THE TIME OF NAIL REMOVAL. THIS IS REPORT 2 OF 5 FOR (B)(4). THIS REPORT IS FOR UNKNOWN NAIL, 8MM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
184502 NAIL, FIXATION, BONE JDS SYNTHES (USA)

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention