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STAR 908-0165Recalls & reported problems

Stryker GmbH · Talar A/P Cut Guide Assembly, Left Small · Class 3

All models of STAR (22)

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 00886385017471), received between May 13, 2019 and May 13, 2019 — classified as 1 malfunction.

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 16, 2026.

Most reported problems

Device problems

  • Break1
  • Fracture1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionMay 13, 2019Break; Fracture; Fracture

    UPON INCOMING INSPECTION, HANDLE WAS BROKEN.

    Patient problems: No Information

    MAUDE report 8605815 ↗

Other Prosthesis, Ankle, Uncemented, Non-Constrained devices

All Prosthesis, Ankle, Uncemented, Non-Constrained devices →

Sources and updates

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