TAPERLOC COMPLETE XR 123 FEMORAL 51-105110Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00880304517127), received between Mar 7, 2022 and May 20, 2026 — classified as 2 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryMay 20, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT APPROXIMATELY THREE YEARS POST-LEFT HIP IMPLANTATION, THE PATIENT RECEIVED TREATMENT FOR TROCHANTERIC BURSITIS. THEY HAD 3 MM LEG LENGTH DISCREPANCY, WHICH IMPROVED FROM PRE-SURGERY. RECEIVED A STEROID INJECTION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Bursitis; Unequal Limb Length

  MAUDE report 25237160 ↗
• MalfunctionFeb 23, 2026Device Contaminated During Manufacture or Shipping

  IT WAS REPORTED THAT DAMAGED STERILE PACKAGING WITH URETHANE IDENTIFIED DURING INSPECTION OF CIRCULATED STOCK ITEMS. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24415659 ↗
• MalfunctionJul 28, 2025Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging

  IT WAS REPORTED DURING INSPECTION OF CIRCULATED ITEMS THAT THE PLASTIC PACKAGING SURROUNDING THE IMPLANT WAS FOUND TO BE DAMAGED. NO ADDITIONAL INFORMATION AVAILABLE FOR THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22628790 ↗
• InjuryMay 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT APPROXIMATELY TWELVE DAYS POST-IMPLANTATION, THE PATIENT UNDERWENT A LEFT HIP REVISION DUE TO A PROXIMAL PERIPROSTHETIC FRACTURE. THE FEMORAL COMPONENT WAS REVISED, AND ADDITIONAL CABLES WERE UTILIZED TO SECURE THE FRACTURE. A NEW BEARING AND HEAD WERE ALSO IMPLANTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Bone Fracture(s)

  MAUDE report 19386891 ↗
• MalfunctionMar 7, 2022Packaging Problem; Packaging Problem

  IT WAS REPORTED CIRCULATED ITEMS WERE INSPECTED AND IDENTIFIED THE STERILE PACKAGE WAS DAMAGED. NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13685197 ↗