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GAMMA 3060-0125SRecalls & reported problems

Stryker GmbH · Lag Screw, Ti · Class 2 · Implant

All models of GAMMA (249)

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 04546540374998), received between Dec 19, 2022 and Dec 19, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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

  • Migration1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryDec 19, 2022Migration; Migration

    IT WAS REPORTED THAT A GAMMA 3 SHS MIGRATED THREE MONTHS AFTER SURGERY, RESULTING IN A REVISION.

    Patient problems: Failure of Implant

    MAUDE report 16010201 ↗

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Sources and updates

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