Masterloc Femoral Stems 01.39.202Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07630030885624), received between Aug 30, 2018 and Oct 24, 2019 — classified as 3 injuries.

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

• InjuryOct 24, 2019Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  THE PATIENT CAME IN COMPLAINING OF PAIN DUE TO NO BONE INGROWTH ON THE STEM. ABOUT 1 YEAR AND 9 MONTHS AFTER PRIMARY THE SURGEON REVISED SUCCESSFULLY THE STEM AND CERAMIC HEAD.

  Patient problems: Pain

  MAUDE report 9233222 ↗
• InjuryJun 5, 2019Unstable

  REVISION SURGERY PERFORMED AFTER 6 MONTHS FROM THE PRIMARY DUE TO INSTABILITY CAUSED BY A SUBSIDED STEM. THE SURGEON REVISED THE STEM, LINER AND HEAD. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Joint Disorder

  MAUDE report 8669897 ↗
• InjuryAug 30, 2018Fracture; Inadequacy of Device Shape and/or Size

  THE PATIENT CAME IN COMPLAINING OF PAIN 21 DAYS AFTER PRIMARY SURGERY. THE SURGEON DETERMINED THAT THE PATIENT HAD A FRACTURED FEMUR. THE SURGEON DETERMINED THAT THE STEM WAS UNDERSIZED IN THE PRIMARY. THE SURGEON REVISED THE STEM AND HEAD. THE SURGERY WAS COMPLETED SUCCESSFULLY

  Patient problems: Bone Fracture(s)

  MAUDE report 7832918 ↗