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MRS 6485-3-813Recalls & reported problems

Howmedica Osteonics Corp. · Curved Cemented Stem · Class 2 · Implant

All models of MRS (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 07613327048605), received between Mar 18, 2021 and Mar 18, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

Patient problems

  • Fall1

Recent adverse event reports

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

  • InjuryMar 18, 2021Fracture; Fracture

    THIS REPORT IS FOR THE REVISION IN (B)(6) 2020 FOR BROKEN STEM, DUE TO FALL. HMRS WAS USED ON (B)(6) 2001. SINCE THE STEM BROKE DUE TO PATIENT FALL IN (B)(6) 2020, IT WAS REPLACED ON (B)(6) 2020. ON (B)(6) 2020, REVISION SURGERY WAS DONE DUE TO INFECTION. PATIENT FELL AGAIN, AND X-RAY SHOWED THAT THE CLIP HAD COME OFF.

    Patient problems: Fall

    MAUDE report 11512686 ↗

Other PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER devices

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Sources and updates

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