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Mpact Acetabular System 01.32.3239HC4Recalls & reported problems

Medacta International SA · Offset 4mm PE HC liner Ø32/C · Class 2 · Implant

All models of Mpact Acetabular System (68)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630040730754), received between Jan 4, 2021 and Apr 25, 2023 — 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

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Appropriate Device Problem Term/Code Not Available1
  • Device Dislodged or Dislocated1

Patient problems

  • Joint Dislocation1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 25, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE PATIENT HAD COMPETITOR COMPONENTS AND CAME IN ON (B)(6) 2023 FOR REASONS UNKNOWN AND THE SURGEON REVISED THE COMPETITOR CUP AND LINER WITH A MEDACTA CUP AND LINER, WITH THE INTENTION OF REVISING THE STEM AND HEAD A WEEK LATER. ON (B)(6) 2023, THE PATIENT CAME BACK IN AND HAD THE COMPETITOR STEM AND HEAD REVISED WITH A MEDACTA STEM AND HEAD. ON (B)(6) 2023, THE PATIENT WAS REVISED IN ORDER TO PUT MORE ANTEVERSION IN STEM AND AN OFFSET LINER WAS IMPLANTED. PRESENTLY, ON (B)(6) 2023, THE PATIENT CAME IN REPORTING INSTABILITY AND THE CAUSE IS UNKNOWN. THE SURGEON REVISED SUCCESSFULLY STEM, HEAD, CUP AND LINER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16806261 ↗
  • InjuryJan 4, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

    THE PATIENT CAME IN AFTER 1 MONTH FROM THE PREVIOUS REVISION SURGERGERY REPORTING PAIN DUE TO A DISLOCATION OF THE HEAD (COMPETITOR) FROM THE LINER (MEDACTA). THE CAUSE OF THE DISLOCATION IS UNKNOWN. THE SURGEON REVISED THE COMPETITOR HEAD AND THE MEDACTA LINER. THE SURGERY WAS COMPLETED SUCCESSFULLY. PREVIOUS REVISION SURGERY REASON WAS STEM MOBILIZATION (THE STEM AND HEAD WERE REVISED).

    Patient problems: Joint Dislocation

    MAUDE report 11106982 ↗

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Sources and updates

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