Masterloc Femoral Stems 01.39.210Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07630030885709), received between Apr 26, 2018 and Sep 10, 2025 — classified as 3 injuries.

The most frequently reported specific device problem is “Osseointegration Problem” (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.

• InjurySep 10, 2025Osseointegration Problem; Osseointegration Problem

  AT 2 YEARS AND 5 MONTHS THE PATIENT CAME IN REPORTING PAIN DUE TO A LOOSE STEM. THE SURGEON REVISED THE MEDACTA STEM AND HEAD WITH A COMPETITOR STEM AND HEAD AND REVISED THE LINER WITH A MEDACTA LINER. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Inadequate Osseointegration

  MAUDE report 23014740 ↗
• InjuryNov 24, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY FOR FEMUR FRACTURE AT ABOUT 10 DAYS FROM PRIMARY SURGERY. THE REASON OF FRACTURE IS UNKNOWN. STEM HEAD AND LINER REVISED SUCCESSFULLY.

  Patient problems: Bone Fracture(s)

  MAUDE report 15860116 ↗
• InjuryApr 26, 2018Appropriate Device Problem Term/Code Not Available

  TWO (2) MONTHS AFTER PRIMARY THE SURGEON REVISED THE PATIENT FOR A FEMORAL FRACTURE HAPPENED DURING PHYSICAL THERAPY. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Hip Fracture

  MAUDE report 7464046 ↗