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Exeter 6309-2-846Recalls & reported problems

Howmedica Osteonics Corp. · RimFit Cup · 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 07613327072136), received between Aug 22, 2022 and Aug 22, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

  • Device Dislodged or Dislocated1

Patient problems

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryAug 22, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED BY THE SALES REP THAT THERE IS REVISION SURGERY - CUP REVISION DUE TO DISLOCATION OF THE HIP AFTER SURGERY IN (B)(6) 2022.

    Patient problems: Joint Dislocation

    MAUDE report 15264539 ↗

Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices

All Prosthesis, hip, semi-constrained, metal/polymer, cemented devices →

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