NAIL, FIXATION, BONE
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
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.
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 |