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REUNION 5901-1111Recalls & reported problems

Stryker GmbH · Extramedullary Resection Guide Assembly · Class 1

All models of REUNION (113)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327099447), received between Mar 14, 2020 and Mar 14, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionMar 14, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS REPORTED THAT DURING A RIGHT REVERSE SHOULDER, THE PIN GOT STUCK IN THE RESECTION GUIDE, AND THE PIN CONNECTOR SNAPPED OFF OF THE GUIDE. REP WAS NOT PRESENT FOR THE PROCEDURE AND DOES NOT KNOW HOW THE ISSUE WAS RESOLVED, BUT IS ABLE TO CONFIRM THE CASE WAS COMPLETED SUCCESSFULLY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9832915 ↗

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Sources and updates

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