Mpact Acetabular System 01.32.148SHRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630030810756), received between Jan 4, 2023 and Jul 9, 2026 — classified as 2 injuries.

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.

• InjuryJul 9, 2026Adverse Event Without Identified Device or Use Problem

  THE PATIENT CAME IN PRESENTING PAIN DUE TO CUP - ILIOPSOAS IMPINGEMENT AND THE CAUSE IS UNKNOWN. IT HAS BEEN REPORTED THAT PROBABLY THE CUP WAS NOT MEDIALIZED ENOUGH AND HAS BEEN MALPOSITIONED, BUT THERE IS NO CONFIRMATION OF THIS INFORMATION. ABOUT 4 YEARS AFTER THE PRIMARY SURGERY, THE SURGEON REVISED THE MEDACTA CUP AND LINER TO COMPETITOR IMPLANTS AND REVISED THE HEAD WITH AN L SIZE AND SLEEVE. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Joint Impingement

  MAUDE report 25763493 ↗
• InjuryJan 4, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT CAME IN REPORTING PAIN AND THE CAUSE IS UNKNOWN. AT ABOUT 1 YEAR AND 1 MONTH POST PRIMARY THE SURGEON REVISED THE MEDACTA CUP AND LINER WITH COMPETITOR COMPONENTS AND REVISED THE MEDACTA HEAD WITH A MEDACTA HEAD. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Implant Pain

  MAUDE report 16094457 ↗