PFNA-II Ø10 130° L240 TAN
Report
- Report Number
- 2520274-2012-03215
- Event Type
- Injury
- Date Received
- November 19, 2012
- Date of Event
- December 27, 2008
- Report Date
- January 26, 2009
- Manufacturer
- SYNTHES
- Product Code
- HSB
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
DEVICE WAS USED FOR TREATMENT. DEVICE IS NOT DISTRIBUTED IN THE UNITED STATES, BUT IS SIMILAR TO DEVICE MARKETED IN THE USA. THIS INDIVIDUAL ADVERSE EVENT REPORT IS BEING MADE IN ACCORDANCE WITH THE SYNTHES MDR EXEMPTION REQUEST DATED OCTOBER 2011. A REVIEW OF THE EVENTS ASSOCIATED WITH THE REQUEST WAS PERFORMED AND IT WAS DETERMINED THAT NONE OF THE EVENTS CONSTITUTES SYSTEMIC ISSUES RELATED TO PRODUCT QUALITY, CHANGES IN PRODUCT DESIGN, METHOD OF USE, OR CHANGES IN EXPECTED RISK THRESHOLDS. REVIEW OF THE DATA ALSO INDICATED NO SIGNIFICANT CHANGE IN RISK/BENEFIT OF EACH PRODUCT CATEGORY, NO EVIDENCE OF DEFICIENCIES IN THE DESIGN, LABELING, OR MANUFACTURE OF THE DEVICE. AS NO LOT NUMBER WAS PROVIDED, NO DEVICE HISTORY RECORD REVIEW CAN BE PERFORMED. THE DEVICE IS NOT BEING RETURNED FOR EVALUATION, NO FURTHER INFORMATION IS AVAILABLE ON THIS EVENT. NO FURTHER INVESTIGATION CAN BE PERFORMED.
(B)(4) COMPLAINT HANDLING UNIT REPORTED A BROKEN NAIL. THE SURGEON USED A PROXIMAL FEMORAL NAIL ANTIROTATION-II SYSTEM FOR A SUBTROCHANTERIC FRACTURE ON (B)(6) 2008. HWB STARTED PARTIALLY ON (B)(6) 2008. THE REHABILITATION WAS CARRIED OUT WITH ONE CRUTCH. THREE MONTHS LATER, A BROKEN NAIL WAS FOUND AT THE PERIODICAL FOLLOW UP. THE DOCTOR SAID THE REDUCTION WOULD NOT BE PROPER, SO THE STRESS WOULD BE LOADED ON THE IMPLANT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PFNA-II Ø10 130° L240 TAN | PFNA-II Ø10 130° | HSB | SYNTHES |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |