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PINNACLE 1217-06-068Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE HIP SOLUTIONS REVISION POROCOAT ACETABULAR SHELL STANDARD 68mm OD 62mm LINER · Class 2 · Implant

All models of PINNACLE (182)

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 10603295008804), received between Oct 7, 2019 and Oct 7, 2019 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryOct 7, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PPF AND STICKER SHEETS RECEIVED. PPF ALLEGES INFECTION. DOI: (B)(6) 2011. (HEAD AND LINER). DOR: (B)(6) 2012 (LEFT HIP). DOI: (B)(6) 2008. (CUP, SCREWS, STEM, AND SLEEVE).

    Patient problems: Unspecified Infection

    MAUDE report 9161926 ↗

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

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Sources and updates

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