MATTA 425757Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540413598), received between Jun 13, 2025 and Jun 13, 2025 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryJun 13, 2025Break; Fracture; Break; Fracture

  IT WAS REPORTED: "PATIENT HAD A PELVIS FX, WE USED A 7 HOLE ANNEALED PLATE TO FIX THE FRACTURE ON (B)(6) 2024. NO MORE THAN 3 WEEKS LATER THE PLATE HAD BROKEN AND WE HAD TO DO A REVISION/ REMOVAL OF THE STRYKER PRODUCT AND REPLACE IT WITH ANOTHER COMPANY'S PRODUCT. PROLONGED HEALING INCURRED".

  Patient problems: Impaired Healing

  MAUDE report 22202598 ↗