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SuperCable® ISO-Elastic™ Cerclage System 35-800-7000Recalls & reported problems

Kinamed, Inc. · Cable Tensioning Instrument, 60° Angled · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
1
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00818720011424), received between Jun 25, 2025 and Jun 25, 2025 — classified as 1 death.

The most frequently reported specific device problem is “Mechanical Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Mechanical Problem1

Patient problems

  • Cardiac Arrest1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • DeathJun 25, 2025Mechanical Problem; Mechanical Problem

    REPORTERS OWN WORDS: STRAIGHT TENSIONER [35-800-2020] WAS BROKEN BEFORE THE START OF THE CASE. THE DEPLOYMENT POST WAS BENT SO UNUSABLE. WE THEN HAD TO USE THE ANGLED TENSIONER WHICH IS DIFFICULT TO USE AND NOT IDEAL. IN THE MIDDLE OF THE CASE IT [ASSUMED TO REFER TO 35-800-7000] FELL APART. WE THEN HAD TO PUT IT BACK TOGETHER ENOUGH SO WE COULD USE IT TO COMPLETE THE CASE. IN TOTAL I [REPORTER] FEEL IT ADDED AN HOUR AT LEAST TO A VERY DIFFICULT PROCEDURE. PATIENT WAS ELDERLY AND UNWELL SO TIME IS IMPORTANT TO GET HIM OUT OF THEATRE AS QUICKLY AS POSSIBLE. PATIENT HAS A PERI PROSTHETIC FRACTURE THAT NEEDED TO BE REPAIRED. AS THE SURGEON WAS APPLYING STAPLES TO CLOSE THE WOUND AT THE END OF THE CASE, THE PATIENT'S CARDIAC STATUS BECAME UNSTABLE. THE TOTAL OPERATION WAS LONG AND COMPLEX, TOOK ABOUT 5 HOURS AND INVOLVED REMOVAL OF A CEMENTED STEM AND IMPLANTATION OF A REVISION STEM. SUBSEQUENT REPORT FROM DISTRIBUTOR: ELDERLY PATIENT UNDERWENT FEMORAL PERI-PROSTHETIC FRACTURE REPAIR PROCEDURE USING CABLE FIXATION, PLATE, AND HIP STEM. DURING THE PROCEDURE THERE WAS A DELAY OF APPROXIMATELY 60 MINUTES DUE TO INSTRUMENT MALFUNCTION. THE REPAIR WAS COMPLETED AND DURING CLOSURE, THE PATIE

    Patient problems: Cardiac Arrest

    MAUDE report 22329672 ↗

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Sources and updates

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