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INSTRUMENT 1020-2730Recalls & reported problems

Howmedica Osteonics Corp. · ACCOLADE NECK TRIAL · Class 2

All models of INSTRUMENT (131)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 07613327208030), received between Jun 5, 2018 and Jun 5, 2018 — classified as 1 malfunction.

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

  • Delamination1

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.

  • MalfunctionJun 5, 2018Delamination; Delamination

    COLOR MARKING FROM THE RASPS CRUMBLE OFF. REPLACEMENT WAS AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7569332 ↗

Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices

All PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices →

Sources and updates

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