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NA 1895-5090SRecalls & reported problems

Stryker GmbH · Condyle Screw · 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 04546540202215), received between Nov 15, 2018 and Nov 15, 2018 — classified as 1 injury.

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 18, 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.

  • InjuryNov 15, 2018Detachment of Device or Device Component

    AT (B)(6) 2018, OPERATION WITH T2SCN WAS DONE. AFTER THE OPERATION, THE END CAP WAS CAME OUT AND THE MOST DISTAL CONDYLE SCREW WAS BACKED OUT. THEREFORE, AT (B)(6) 2018, THE END CAP AND CONDYLE SCREW WAS REMOVED AND NEW SAME DEVICES WERE IMPLANTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8075180 ↗

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

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Sources and updates

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