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MEDPOR 5444-1-310Recalls & reported problems

Stryker Leibinger GmbH & Co. KG · MEDPOR CUSTOMIZED-PLUS-L · Class 2 · Implant

All models of MEDPOR (25)

Data updated Oct 18, 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 07613327300420), received between Aug 30, 2018 and Aug 30, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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 18, 2026.

Most reported problems

Device problems

  • Patient-Device Incompatibility1

Patient problems

  • No Code Available1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryAug 30, 2018Patient-Device Incompatibility

    IT WAS REPORTED BY A COMPANY REPRESENTATIVE THAT AFTER AN INITIAL SURGERY WAS COMPLETED A REVISION SURGERY TOOK PLACE TO REMOVE THE IMPLANT DUE TO AN INFECTION. THE INFECTION WAS TREATED. NO ADDITIONAL INFORMATION IS AVAILABLE REGARDING THE INFECTION. MEDICAL INTERVENTION AND ADVERSE CONSEQUENCES OF THE REVISION SURGERY ARE UNKNOWN.

    Patient problems: No Code Available; Unspecified Infection

    MAUDE report 7834272 ↗

Other PROSTHESIS, CHIN, INTERNAL devices

All PROSTHESIS, CHIN, INTERNAL devices →

Sources and updates

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