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REUNION 5901-S-5217Recalls & reported problems

Stryker GmbH · Single Radius Humeral Head Trial · Class 1

All models of REUNION (113)

Data updated Oct 18, 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 07613327100075), received between Nov 19, 2018 and Sep 3, 2019 — classified as 2 malfunctions.

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

Most reported problems

Device problems

  • Break1
  • Naturally Worn1

Patient problems

  • No Known Impact Or Consequence To Patient1
  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionSep 3, 2019Naturally Worn

    UPON INCOMING INSPECTION, ITEMS WERE VISIBLY WORN. NO ASSOCIATED PROCEDURE.

    Patient problems: No Patient Involvement

    MAUDE report 8958193 ↗
  • MalfunctionNov 19, 2018Break

    BROKEN NUMERAL HEAD TRIAL OBSERVED INTRAOPERATIVELY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8084270 ↗

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Sources and updates

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