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PINNACLE GRIPTION 1217-30-072Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE GRIPTION ACETABULAR SHELL MULTI-HOLE 72mm OD · Class 2 · Implant

All models of PINNACLE GRIPTION (57)

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 10603295010081), received between Sep 4, 2018 and Sep 4, 2018 — classified as 1 malfunction.

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

  • Appropriate Device Problem Term/Code Not Available1

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.

  • MalfunctionSep 4, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    THE (B)(6) CODED PRODUCT'S USAGE INFORMATION WAS RECEIVED FROM THE HOSPITAL FOR (B)(4) LOT NUMBER, HOWEVER IN THE SYSTEM HOSPITAL WAS SOLD HJ4056 LOT NUMBER. IT IS BELIEVED THE INSIDE AND OUTSIDE BAR CODES ARE NOT MATCHING.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7841634 ↗

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

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

Sources and updates

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