3.0MM TI HEADLESS COMPRESSION SCREW 18MM/SHORT THREAD-STER
Report
- Report Number
- 2520274-2013-00530
- Event Type
- Malfunction
- Date Received
- January 22, 2013
- Date of Event
- August 3, 2009
- Report Date
- August 13, 2009
- Manufacturer
- SYNTHES
- Product Code
- HWC
- PMA / PMN Number
- K050636
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
DEVICE WAS USED FOR TREATMENT. 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 THE TIP BROKE OFF DURING INSERTION. THE PATIENT HAD DIABETES. AFTER PRE-DRILLING, THE SURGEON INSERTED THE HEADLESS COMPRESSION SCREW TO THE DISTAL FIBULA. AT THAT TIME, THE SURGEON COULD HEAR NOISE BREAKING SOMETHING METAL. THE TIP OF THE SCREW WAS BROKEN. THE X-RAY PHOTO SHOWED THE FRAGMENT FROM THE SCREW IN THE FIBULA. THE DOCTOR DECIDED TO LEAVE THE SCREW IN THE FIBULA.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 30204 | 3.0MM TI HEADLESS COMPRESSION SCREW 18MM/SHORT THREAD-STER | 3.0MM TI HEADLESS COMPRESSION | HWC | SYNTHES |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |