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Exeter 6309-3-652Recalls & reported problems

Howmedica Osteonics Corp. · RimFit Cup · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327072280), received between Mar 27, 2018 and Mar 27, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment Of Device Component” (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

  • Detachment Of Device Component1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionMar 27, 2018Detachment Of Device Component; Detachment Of Device Component

    CUSTOMER NOTICED THAT 2 CEMENT SPACERS HAD FALLEN OF THE IMPLANT WHEN OPENING THE BOX. THEY THEN OPENED ANOTHER AND USED THAT ONE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7373974 ↗

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.