CONSERVE® 38AC4600Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M68438AC46001), received between Apr 20, 2022 and Apr 20, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

• InjuryApr 20, 2022Device Dislodged or Dislocated

  ALLEGEDLY, PLAINTIFF RECEIVED A WRIGHT HIP SYSTEM ON (B)(6) 2010. AFTER IMPLANTATION OF THE WRIGHT HIP SYSTEM, PLAINTIFF BEGAN SUFFERING PERSISTENT PAIN AND DECREASED MOBILITY, BOTH WORSENING OVER TIME. PLAINTIFFS WRIGHT HIP SYSTEM DETACHED, DISCONNECTED, CREATED METALLIC DEBRIS, RELEASED METAL IONS, AND/OR LOOSENED FROM PLAINTIFF? ACETABULUM, LOOSENING THROUGH OSTEOLYSIS, INFLAMMATION CAUSING DAMAGE OR DEATH TO TISSUE AND BONE AROUND THE IMPLANT AND METALLOSIS. ON (B)(6) 2021, PLAINTIFF WAS REQUIRED TO UNDERGO REVISION SURGERY TO REMOVE AND REPLACE WRIGHT HIP SYSTEM.

  Patient problems: Metal Related Pathology; Osteolysis; Pain

  MAUDE report 14160306 ↗