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TELEGRAPH® EVOLUTION Humeral Nailing System 270812 - TELEGRAPH EVOLUTION CANNULATED CONNECTING SCREW FOR NAILRecalls & reported problems

Fournitures Hospitalieres Industrie · Class 1

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

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 03661489708121), received between Sep 28, 2023 and Mar 13, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (3 reports).

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: 1 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 1 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: 0 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: 1 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

  • Break3
  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 13, 2026Break

    BREAKAGE OF THE THREADING OF THE CONNECTION SCREW WITH THE NAILING HOOP STUCK IN THE THREAD OF THE NAIL IN PLACE. IT IS IMPOSSIBLE TO REMOVE THIS PIECE, WHICH OBSTRUCTS THE CONDUIT AND PREVENTS THE NAIL FROM BEING EXTRACTED. AFTER NUMEROUS ATTEMPTS WITH A BROKEN SCREW DRIVER, THE NAIL CANNOT BE REMOVED EXCEPT BY AGGRESSIVELY RELEASING THE FIRST CENTIMETRE, WITH AN UNFAVOURABLE RISK/BENEFIT RATIO.THE PROXIMAL SCREWS WERE LEFT IN PLACE TO PREVENT THE NAIL FROM MIGRATING INTRAMEDULLARY.REMOVAL OF THE DISTAL SCREWS AND CLOSURE. THE NAIL COULD NOT BE REMOVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24590338 ↗
  • MalfunctionApr 19, 2024Break; Break

    DURING THE SURGERY, THE SCREW HOLDING THE NAIL TO THE NAIL HOLDER BROKE INSIDE THE IMPLANT. DESPITE THIS, WE MANAGED TO REMOVE THE BROKEN SCREW THREAD FROM THE IMPLANT.THE IMPLANT COULD FINALLY BE USED BECAUSE THE TEAM MANAGED TO EXTRACT THE BROKEN SCREW FRAGMENT. AT THE END OF THE OPERATION, THERE WAS NO PROXIMAL OR DISTAL TARGETING DEVICE, WHICH MADE IT DIFFICULT TO LOCK THE NAIL. IN THE END, THE SURGEON WAS ABLE TO INSERT 1 PROXIMAL SCREW BUT NO DISTAL SCREW. INCREASE IN OPERATING TIME: THE OPERATION LASTED APPROXIMATELY 3 HOURS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19141987 ↗
  • MalfunctionJan 19, 2024Break; Break

    CONNECTION SCREW BROKEN IN THE NAIL. THE NAIL HAD TO BE TAKEN OUT BECAUSE IT WAS TOO DEEP AND A NEW ONE PUT IN. LOSS OF TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18543750 ↗
  • MalfunctionSep 28, 2023Fracture; Fracture

    DURING A SURGICAL PROCEDURE, A CENTROMEDULAR NAILING OF THE HUMERUS USING A NEW TRIAL ANCILLARY (TELEGRAPH LONG FH NAIL) THE NAIL HOLDER BROKE AT THE LEVEL OF THE SCREW THREAD, REMAINING IN THE NAIL. DIFFICULTY TO BE EXPECTED WHEN REMOVING OSTEOSYNTHESIS MATERIAL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17834667 ↗

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Sources and updates

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