Mpact Acetabular System 01.32.150MHTRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630345798756), received between Jun 9, 2026 and Jun 9, 2026 — classified as 1 injury.

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 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 9, 2026Osseointegration Problem

  AT ABOUT 20 DAYS FROM THE PRIMARY, THE PATIENT CAME IN PRESENTING PAIN AND INSTABILITY DUE TO A LOOSE CUP AND THE CAUSE IS UNKNOWN. THERE WERE NO REPORTS OF TRAUMA OR A FALL. THE SURGEON REVISED THE AMISTEM-P SIZE00 TO A LAT. SIZE0, THE BIOLOX HEAD TO A SAME-SIZE HEAD, THE MPACT D 50 MULTI-HOLE CUP TO A D 54 CUP, AND THE FLAT PE HC LINER D 36/E TO A D 36/F LINER. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Aseptic loosening; Inadequate Osseointegration

  MAUDE report 25442528 ↗