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OMEGA 597144SRecalls & reported problems

Stryker GmbH · Standard Barrel Hip Plate; Keyless · Class 2 · Implant

All models of OMEGA (20)

Data updated Oct 16, 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 07613154325566), received between Jul 12, 2019 and Jul 12, 2019 — classified as 1 injury.

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

  • Fracture1

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.

  • InjuryJul 12, 2019Fracture

    PATIENT IN (B)(6) 2018 HAD A HIP FRACTURE AND HAD AN OMEGA PLATE/LAG SCREW AS WELL 7.2 CANNULATED SCREW. HARDWARE WAS REMOVED PRIOR TO STARTING THA PROCEDURE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8784565 ↗

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices

All APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices →

Sources and updates

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