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Conformis Hip System HCC032B05601Recalls & reported problems

Conformis, Inc. · ACETABULAR CUP, PLASMA SPRAY 56 · Class 2 · Implant

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 M572HCC032B056011), received between Aug 11, 2020 and Aug 11, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Malposition of Device” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Malposition of Device1
  • Unintended Movement1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryAug 11, 2020Malposition of Device; Unintended Movement

    IT WAS REPORTED THAT THE SURGEON NOTICED THAT THE CUP HAD SHIFTED RIGHT BEFORE CLOSING UP THE PATIENT. IT WAS NOTED THAT THE SURGEON DOESN'T USE SCREWS FOR MOST CASES. THE SURGEON HAD TO REMOVE THE LINER FROM THE CUP AND REPOSITION IT USING SCREWS TO SUCCESSFULLY COMPLETE THE SURGERY, BUT THE ISSUE RESULTED IN A 45 MINUTE DELAY IN THE PROCEDURE.

    Patient problems: No Code Available

    MAUDE report 10393037 ↗

Other Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented devices

All Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.