ARTICUL/EZE 4734-40-120Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295505785), received between Jun 10, 2024 and Jul 27, 2026 — classified as 3 injuries.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that the patient showed signs of possible infection. Doctor washed out the hip and exchanged the head and liner.DOI: Unknown,DOR: Unknown,Affected side: Left Hip.

  Patient problems: Unspecified Infection

  MAUDE report 50012649 ↗
• InjuryMar 5, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THEY HAD TO EXPLANT ALL IMPLANTS BECAUSE PATIENT WAS UNSTABLE DOI: (B)(6) 2026. DOR: (B)(6) 2026. AFFECTED SIDE: RIGHT HIP.

  Patient problems: Joint Laxity

  MAUDE report 24518349 ↗
• InjuryJun 10, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  STUDY NO: DOTS CLINICAL NOTIFICATION RECEIVED FOR REVISION DUE TO DISLOCATION. DATE OF IMPLANT: (B)(6) 2023 DATE OF REVISION: (B)(6) 2024 (LEFT HIP). TREATMENT: HEAD AND LINER WERE REVISED.

  Patient problems: Joint Dislocation

  MAUDE report 19498552 ↗