Exactech 170-36-50Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885862155573), received between Mar 9, 2021 and Aug 8, 2023 — classified as 2 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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryAug 8, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A 66 YO FEMALE PATIENT, WHO HAD AN INITIAL RIGHT HIP IMPLANTED ON (B)(6), 2015, AND WAS REVISED ON (B)(6), 2023, UNDERWENT A SECOND REVISION PROCEDURE ON (B)(6), 2023. THE PATIENT PRESENTED TO THE SURGEON DUE TO A DISLOCATION. THEY UNDERWENT A TOTAL HIP ACETABULAR REVISION USING DJO DUAL MOBILITY. THE PATIENT FEMORAL HEAD WAS REPLACED WITH A SLEEVE AND A NEW HEAD TO MATCH THE DJO DUAL MOBILITY. THERE WERE NO DEVICE BREAKAGES REPORTED. THERE WAS A 15-TO-30-MINUTE SURGICAL DELAY DURING THE PROCEDURE WITH NO ADVERSE EVENT TO THE PATIENT AS A RESULT. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. X-RAYS AND DEVICE IMAGES WERE PROVIDED. NO DEVICE RETURNS ANTICIPATED BECAUSE THEY WERE SENT TO THE LAB AND LEGAL AT THE HOSPITAL.

  Patient problems: Joint Dislocation

  MAUDE report 17480061 ↗
• InjuryMar 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED, APPROXIMATELY 6 MONTHS POSTOP A RIGHT HIP REVISION, THE (B)(6) Y/O FEMALE PATIENT DEVELOPED LAXITY IN HER RIGHT HIP. THE SURGEON UPSIZED THE FEMORAL HEAD AND ACHIEVED BETTER TENSION IN THE JOINT. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. THE DEVICE WILL NOT BE RETURNED FOR EVALUATION DUE TO HOSPITAL THREW DEVICE AWAY.

  Patient problems: Failure of Implant

  MAUDE report 11445122 ↗