Mpact Acetabular System 01.32.162MHRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630030810985), received between May 26, 2021 and Jan 9, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 9, 2024Osseointegration Problem; Osseointegration Problem

  THE PATIENT HAD A PRIMARY HIP SURGERY WITH A COMPETITOR AT AN UNKNOWN DATE. SUBSEQUENTLY, THE PATIENT WAS REVISED FOR AN UNKNOWN REASON AND A MEDACTA CUP, HEAD AND LINER WERE IMPLANTED ON (B)(6) 2023. PRESENTLY, ON (B)(6) 2023 THE PATIENT CAME IN REPORTING PAIN DUE TO A LOOSE CUP. THE SURGEON REVISED THE MEDACTA CUP AND LINER WITH A COMPETITOR'S PRODUCT AND REVISED THE MEDACTA HEAD WITH ANOTHER MEDACTA HEAD. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Implant Pain

  MAUDE report 18474064 ↗
• InjuryMay 26, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

  THE PATIENT CAME IN REPORTING PAIN DUE TO A CUP DISLOCATION, THE CUP CAME OUT OF BONE. THE CAUSE OF THE CUP DISLOCATION IS UNKNOWN. THE SURGEON REVISED THE CUP AND LINER WITH COMPETITOR HARDWARE AND REVISED THE MEDACTA HEAD WITH A MEDACTA HEAD AND ADDED A SLEEVE ALMOST 1 MONTH AND A HALF AFTER PRIMARY. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Inadequate Osseointegration

  MAUDE report 11885937 ↗