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MATTA 425768Recalls & reported problems

Stryker GmbH · Straight Acetabular Plate · Class 2 · Implant

Data updated Oct 13, 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 04546540413703), received between Jun 15, 2018 and Jun 15, 2018 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • 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.

  • InjuryJun 15, 2018Fracture

    ORIF OF FRACTURE OF THE PELVIS RING WITH USE OF STRYKER PLATES (MATTA, 18 HOLES FLEXPLATE). THE RECEIVED PHOTO CONFIRMS THE PLATE TO BE BROKEN.

    Patient problems: No Information

    MAUDE report 7607269 ↗

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

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Sources and updates

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