FDA Adverse Event Injury Summary report: N

NAIL, FIXATION, BONE

MDR report key: 4109064 · Received September 23, 2014

Report

Report Number
2520274-2014-13710
Event Type
Injury
Date Received
September 23, 2014
Date of Event
April 15, 2014
Report Date
September 3, 2014
Manufacturer
SYNTHES (USA)
Product Code
JDS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS LU, C.-C. ET AL (2014) COMPLICATIONS AND TECHNICAL PITFALLS OF TITANIUM ELASTIC NAIL FIXATION FOR MIDCLAVICULAR FRACTURES. ORTHOPEDICS 37(4), E377-E383. THIS REPORT IS FOR AN UNKNOWN TITANIUM ELASTIC NAIL. 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.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING JOURNAL ARTICLE: LU, C.-C. ET AL (2014) COMPLICATIONS AND TECHNICAL PITFALLS OF TITANIUM ELASTIC NAIL FIXATION FOR MIDCLAVICULAR FRACTURES. ORTHOPEDICS 37(4), E377-E383. FROM JANUARY 2007 TO APRIL 2008, 27 PATIENTS (17 MEN, 10 WOMEN; MEAN AGE 45.8 YEARS; RANGE 16.5-66.9 YEARS) WITH MARKED DISPLACED MIDCLAVICULAR FRACTURES UNDERWENT FIXATION WITH TITANIUM ELASTIC NAILS (SYNTHES, (B)(4)). NO INFECTION, NONUNION, NAIL DISLOCATION, OR IMPLANT BREAKAGE OCCURRED AND ALL PROCEDURES HEALED WITHOUT SECONDARY PROCEDURES. COMPLICATIONS INCLUDED 1 PATIENT WITH MISPLACED NAIL INSERTION THAT REQUIRED REVISION, 3 PATIENTS WITH MEDIAL NAIL TIP IRRITATION, IATROGENIC PERFORATION OF THE POSTEROLATERAL CORTEX OCCURRED IN 2 PATIENTS WITHOUT A REPORTED PRODUCT PROBLEM, AND 1 PATIENT WITH IATROGENIC PERFORATION OF THE POSTEROLATERAL CORTEX WITH ENTRY POINT PAIN AND MEDIAL NAIL TIP PROMINENCE WITH IMPLANT REMOVAL. THIS IS REPORT 3 OF 4 FOR (B)(4). THIS COMPLAINT IS FOR AN UNKNOWN TITANIUM ELASTIC NAIL. A COPY OF THE JOURNAL ARTICLE IS BEING SUBMITTED WITH THIS MEDWATCH. THIS REPORT IS FOR 14 DEVICES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
592429 NAIL, FIXATION, BONE JDS SYNTHES (USA)

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention