FDA Adverse Event Malfunction Summary report: N

3.0MM TI HEADLESS COMPRESSION SCREW 18MM/SHORT THREAD-STER

MDR report key: 2924443 · Received January 22, 2013

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

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

(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