Trident 502-01-50DRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613153073079), received between May 28, 2019 and Apr 5, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryApr 5, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  PATIENT HAD A CONSTRAINED LINER IMPLANTED TO ADDRESS RECURRING DISLOCATIONS. THE LINER DETACHED FROM THE ACETABULAR SHELL. THE CUP WAS REMOVED AND A MULTIHOLE CUP WAS IMPLANTED IN A DIFFERENT POSITION AND A MDM CONSTRUCT WAS DEEMED STABLE.

  Patient problems: Ambulation or Postural Difficulties

  MAUDE report 14018056 ↗
• InjuryMar 31, 2020Loss of Osseointegration; Loss of Osseointegration

  ASEPTIC LOOSENING TRIDENT ACETABULAR COMPONENT. PATIENT REQUIRED REVISION OF ACETABULAR COMP.

  Patient problems: Inadequate Osseointegration; Injury

  MAUDE report 9903681 ↗
• InjuryMay 28, 2019Osseointegration Problem; Osseointegration Problem

  THE FOLLOWING REVISION EVENT WAS INCLUDED IN A REPORT RECEIVED AS PART OF THE (B)(6): PATIENT HAD A RIGHT PRIMARY THA DUE TO AVASCULAR NECROSIS; UNDERWENT REVISION DUE TO ASEPTIC LOOSENING OF THE ACETABULAR COMPONENT. THE CUP, LINER AND HEAD WERE EXCHANGED. PATIENT'S BMI IS REPORTED AS 30.1.

  Patient problems: Inadequate Osseointegration; Injury

  MAUDE report 8645732 ↗