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PINNACLE 2217-00-060Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE ALTER BEARING EXTRACTOR BODY 60mm · Class 1

All models of PINNACLE (182)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295097327), received between Mar 2, 2021 and Jul 7, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 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

  • Break2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 7, 2021Break; Break

    AT LEAST ON OF THE TIPS OF EACH OF THE AB EXTRACTOR IS BROKEN . UNKNOWN CIRCUMSTANCES, ISSUE RAISED BY STERILE SERVICES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12129953 ↗
  • MalfunctionMar 2, 2021Break; Break

    ROUTINE INSPECTION INDICATED BROKEN TIP. DELAY 5 MINUTES. NO ISSUE TO PATIENT. SPARE WAS AVAILABLE. PRODUCT DISCARDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11398997 ↗

Other WRENCH devices

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Sources and updates

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