Mpact Acetabular System 01.32.148MHRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630030810749), received between Jan 21, 2019 and Jan 5, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Activation, Positioning or Separation 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJan 5, 2021Activation, Positioning or Separation Problem

  AFTER INSERTING MPACT 48MM AT THE PATIENT ACETABULAR, THE SURGEON TRIED TO ENGAGE MPACT LINER WITH MPACT CUP, BUT THE SURGEON WAS NOT ABLE TO. THE SURGEON CHECKED THE INSIDE AND THE OUTSIDE OF THE MPACT CUP AND TRIED TO ENGAGE THE SAME MPACT LINER, BUT THE SURGEON WAS NOT ABLE TO. THE SURGEON REPLACED WITH A NEW MPACT LINER WHICH WAS THE SAME REFERENCE AND THE DIFFERENT LOT, BUT THE SURGEON WAS NOT ABLE TO ENGAGE AGAIN. THE SURGEON FINALLY REPLACED IT WITH A NEW MPACT CUP 50MM AND A NEW LINER. REPLACED MPACT LINER WAS ABLE TO ENGAGE WITH REPLACED MPACT CUP AS USUAL. TOTAL SURGERY TIME WAS ABOUT 2 HOURS WITH 45MINUTES OF DELAY.

  Patient problems: Insufficient Information

  MAUDE report 11115884 ↗
• InjuryJan 21, 2019Device Dislodged or Dislocated

  ON (B)(6) 2018 WE WERE INFORMED THAT A PATIENT WAS REVISED 4 WEEKS AFTER PRIMARY DUE TO CUP DISLOCATION.

  Patient problems: No Code Available

  MAUDE report 8264000 ↗