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Mpact Acetabular System 01.32.146SHRecalls & reported problems

Medacta International SA · Acetabular shell Ø46 No-hole · 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 07630030810725), received between Sep 26, 2017 and Sep 26, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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

  • Loose or Intermittent Connection1

Patient problems

  • Joint Disorder1
  • Pain1

Recent adverse event reports

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

  • InjurySep 26, 2017Loose or Intermittent Connection

    THE PATIENT CAME IN COMPLAINING OF PAIN. THE SURGEON DETERMINED THE CUP WAS LOOSE. THE CAUSE OF LOOSENING IS UNKNOWN. NO REPORT OF TRAUMA. THE SURGEON REVISED THE CUP, HEAD AND LINER. THE SURGEON RE-IMPLANTED WITH MEDACTA PRODUCT. THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Joint Disorder; Pain

    MAUDE report 6893676 ↗

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

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

Sources and updates

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