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PINNACLE POROCOAT 1217-20-066Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE POROCOAT ACETABULAR SHELL MULTI-HOLE II 66mm OD · Class 3 · Implant

All models of PINNACLE POROCOAT (38)

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 10603295009696), received between Oct 17, 2019 and Oct 17, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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

  • Loss of Osseointegration1
  • Osseointegration Problem1

Patient problems

  • Discomfort1
  • Inadequate Osseointegration1
  • Pain1

Recent adverse event reports

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

  • InjuryOct 17, 2019Loss of Osseointegration; Osseointegration Problem; Loss of Osseointegration; Osseointegration Problem

    LITIGATION ALLEGES LOOSENING OF THE CUP AND STEM. DOI: (B)(6) 2005; DOR: (B)(6) 2011; (RIGHT HIP).

    Patient problems: Discomfort; Inadequate Osseointegration; Pain

    MAUDE report 9202914 ↗

Other Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented devices →

Sources and updates

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