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KinematX 115-11000-SRecalls & reported problems

Extremity Medical, LLC · KinematX Radial Stem - Size 1; Sterile Packed · Class 2 · Implant

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842078111512), received between Dec 2, 2022 and Dec 2, 2022 — classified as 1 injury.

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 Problem1

Patient problems

  • Implant Pain1

Recent adverse event reports

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

  • InjuryDec 2, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    SURGEON REPORTED THAT A PATIENT WAS EXPERIENCING PAIN IN HIS WRIST WHILE IN EXTENSION. A REVISION SURGERY WAS SUCCESSFULLY COMPLETED TO EXCHANGE THE RADIAL STEM AND RADIAL BODY.

    Patient problems: Implant Pain

    MAUDE report 15905756 ↗

Other Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained devices

All Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained devices →

Sources and updates

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