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Distal Elbow Plating System Proximal Ulna Plate, 73mm, RightRecalls & reported problems

Skeletal Dynamics L.L.C. · Class 2 · Implant

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

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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841506105772), received between May 7, 2021 and May 7, 2021 — classified as 2 injuries.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem2

Patient problems

  • Bone Fracture(s)2

Recent adverse event reports

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

  • InjuryMay 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE FRACTURE DISPLACED POST-OPERATIVELY. IMPLANT WAS REMOVED AND REPLACED.

    Patient problems: Bone Fracture(s)

    MAUDE report 11792576 ↗
  • InjuryMay 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE FRACTURE DISPLACED POST-OPERATIVELY. IMPLANT WAS REMOVED AND REPLACED.

    Patient problems: Bone Fracture(s)

    MAUDE report 11792531 ↗

Other Plate, fixation, bone devices

All Plate, fixation, bone devices →

Sources and updates

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