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PINNACLE 2217-00-044Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE ALTER BEARING EXTRACTOR BODY 44mm · Class 1

All models of PINNACLE (182)

Data updated Oct 16, 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 10603295097242), received between Jul 10, 2019 and Jul 10, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Code Available1
  • 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.

  • MalfunctionJul 10, 2019Break; Break

    AFTER REVIEW OF MEDICAL RECORDS PATIENT WAS REVISED TO ADDRESSED LEFT HIP REPLACEMENT METAL ON METAL WITH INCREASING SERUM CHROMIUM AND COBALT LEVELS HOWEVER LABORATORY RESULT REPORTED WITHIN NORMAL LEVEL. PATIENT ALLEGED PAIN. DOI: (B)(6) 2011 DOR: (B)(6) 2019 LEFT HIP.

    Patient problems: No Code Available; No Consequences Or Impact To Patient

    MAUDE report 8775955 ↗

Other WRENCH devices

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Sources and updates

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