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Sidus® Stem-Free Shoulder 01.04555.520Recalls & reported problems

Zimmer GmbH · Class 2 · Implant

All models of Sidus Stem-Free Shoulder (9)

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 00889024415997), received between Mar 14, 2019 and Mar 14, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Remove” (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

  • Difficult to Remove1
  • Physical Resistance/Sticking1

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.

  • InjuryMar 14, 2019Difficult to Remove; Physical Resistance/Sticking; Difficult to Remove; Physical Resistance/Sticking

    IT WAS REPORTED THAT DURING THE SURGERY THE FORK WEDGED BETWEEN THE ANCHOR AND HEAD. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8421030 ↗

Other Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained devices

All Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained devices →

Sources and updates

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