AEQUALIS RESURFACING HEAD DWD805Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 03700386926952), received between Jan 9, 2017 and Oct 25, 2019 — classified as 3 injuries.

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.

• InjuryOct 25, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION SURGERY FOR PAIN 17 MONTHS AFTER PRIMARY SURGERY. PATIENT ID: (B)(6).

  Patient problems: Pain

  MAUDE report 9241730 ↗
• InjuryOct 25, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT HAD AN ADVERSE EVENT DESCRIBED AS "SUBLUXATION/DISLOCATION OF THE STUDY SHOULDER RELATED TO SEIZURE" 2 YEARS AFTER PRIMARY SURGERY. PATIENT ID: (B)(6).

  Patient problems: Joint Dislocation

  MAUDE report 9241728 ↗
• InjuryJan 9, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION SURGERY AT 6 YEARS POST-OPERATIVE DUE TO GLENOID ARTHROSIS. CONVERSION TO TSA.

  Patient problems: Patient Problem/Medical Problem

  MAUDE report 6232254 ↗