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PINNACLE GRIPTION 1217-17-064Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE GRIPTION ACETABULAR SHELL REVISION (DPX) 64mm OD 58 LINER · Class 2 · Implant

All models of PINNACLE GRIPTION (57)

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

Adverse event reports
6
Deaths reported
0
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295009504), received between Oct 13, 2017 and Apr 13, 2023 — classified as 6 injuries.

The most frequently reported specific device problem is “Loss of Osseointegration” (3 reports).

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 Osseointegration3
  • Adverse Event Without Identified Device or Use Problem1
  • Osseointegration Problem1
  • Use of Device Problem1

Patient problems

  • Inadequate Osseointegration4
  • No Code Available3
  • Pain2
  • No Information1
  • Not Applicable1
  • Unspecified Infection1

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 13, 2023Use of Device Problem; Use of Device Problem

    THE PATIENT WAS REVISED DUE TO HIP PAIN AND MISPLACED CUP. DOI: UNKNOWN. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT HIP.

    Patient problems: Pain

    MAUDE report 16730898 ↗
  • InjuryApr 2, 2020Loss of Osseointegration; Loss of Osseointegration

    REVISION OF ACETABULAR COMPONENT DUE TO ASEPTIC LOOSENING.

    Patient problems: Inadequate Osseointegration; No Code Available

    MAUDE report 9917754 ↗
  • InjuryAug 19, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    PPF ALLEGES DISLOCATION WITH CLOSED REDUCTION AND INFECTION REQUIRING INTRAVENOUS ANTIBIOTICS. ADDED LAWYER, LAW FIRM, EXPIRATION DATES AND PATIENT HARM. LITIGATION CHECK BOX IS NOW TICKED. CORRECTED PATIENT IDENTIFIER. ADDED CUP AND HOLE ELIMINATOR DUE TO ALLEGED INFECTION. DOI: (B)(6) 2013 - DOR: (B)(6) 2014 (RIGHT HIP, THIRD REVISION).

    Patient problems: No Code Available; Unspecified Infection

    MAUDE report 8905809 ↗
  • InjuryApr 12, 2019Loss of Osseointegration; Loss of Osseointegration

    PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE CUP AT BONE TO IMPLANT INTERFACE WITH BROKEN SCREWS RESULTING IN FLUID COLLECTION AND PAIN.

    Patient problems: Inadequate Osseointegration; No Code Available; Pain

    MAUDE report 8510419 ↗
  • InjuryJun 12, 2018Osseointegration Problem; Osseointegration Problem

    PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE CUP COMPONENT AT BONE TO IMPLANT INTERFACE. REMOVED CUP AND LINER AND IMPLANTED NEW CUP.  DOI: UNKNOWN; DOR: (B)(6) 2018; RIGHT HIP.

    Patient problems: Inadequate Osseointegration; Not Applicable

    MAUDE report 7591802 ↗
  • InjuryOct 13, 2017Loss of Osseointegration; Loss of Osseointegration

    THE PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE ACETABULAR CUP AT THE BONE TO IMPLANT INTERFACE.

    Patient problems: Inadequate Osseointegration; No Information

    MAUDE report 6948987 ↗

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

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

Sources and updates

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