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Mpact Acetabular System 01.32.3252HCTRecalls & reported problems

Medacta International SA · Flat PE HC liner Ø 32 /G · Class 2 · Implant

All models of Mpact Acetabular System (68)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030811999), received between Dec 21, 2018 and Dec 21, 2018 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryDec 21, 2018Appropriate Device Problem Term/Code Not Available

    THE PATIENT CAME IN COMPLAINING OF PAIN 1 YEAR AND 8 MONTHS AFTER PRIMARY. THE SURGEON REVISED THE STEM AND HEAD WITH ANOTHER COMPANY'S PRODUCT. THE LINER WAS REVISED WITH A MEDACTA LINER AND THE SURGERY WAS COMPLETED SUCCESSFULLY. THE REASON OF THE PAIN IS UNKNOWN. IT WAS THOUGHT THAT THE PATIENT MAY BE INFECTED DUE TO SWELLING. THE FROZEN AND MICRO PATHOLOGY REPORTS CAME BACK NEGATIVE.

    Patient problems: Pain

    MAUDE report 8188867 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices

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Sources and updates

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