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NA 394.796Recalls & reported problems

Synthes GmbH · 11.0MM CARBON FIBER BRIDGING ROD 190MM SHORT · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982199812), received between Oct 31, 2025 and Oct 31, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

2 other recalls cover devices cleared under the same FDA submission (K122455); they may or may not involve this specific model.

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 16, 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: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 2 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 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break2
  • Contamination /Decontamination Problem2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 31, 2025Break; Contamination /Decontamination Problem; Break; Contamination /Decontamination Problem

    IT WAS REPORTED ON AN UNKNOWN DATE, ITEMS NEED REPLACING, THE DRILL SLEEVES CATCH. THERE IS WHITE RESIDE ON THE BARS AND CHIPS ON THE BARS, 4.0 ADAPTERS DO NOT WORK. THERE WERE NO ADVERSE EVENTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23442066 ↗
  • MalfunctionOct 31, 2025Break; Contamination /Decontamination Problem; Break; Contamination /Decontamination Problem

    IT WAS REPORTED ON AN UNKNOWN DATE, ITEMS NEED REPLACING, THE DRILL SLEEVES CATCH. THERE IS WHITE RESIDE ON THE BARS AND CHIPS ON THE BARS, 4.0 ADAPTERS DO NOT WORK. THERE WERE NO ADVERSE EVENTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23442062 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K122455. One submission often covers many models, so check the product and lot details in each record.

  • Z-2451-2015 · Jul 29, 2015 · Terminated
    Synthes Trauma Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended to stabilize and provide treatment for fractures of the small bones, such as th
  • Z-1833-2014 · Apr 10, 2014 · Terminated
    Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components.

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices

All APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page