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PINNACLE 2217-00-066Recalls & reported problems

Depuy Orthopaedics, Inc. · PINNACLE ALTER BEARING EXTRACTOR BODY 66mm · 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 10603295097358), received between May 24, 2019 and Apr 27, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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 18, 2026.

Most reported problems

Device problems

  • Device-Device Incompatibility1
  • Material Twisted/Bent1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionApr 27, 2021Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED THAT SCREW PIN, SPRING AND SUCTION CUP STRIPPED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11732441 ↗
  • MalfunctionMay 24, 2019Device-Device Incompatibility; Device-Device Incompatibility

    EXTRACTOR DEFICIENCY IS THAT THE LEVER DOESN¿T HOLD.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8640295 ↗

Other EXTRACTOR devices

All EXTRACTOR devices →

Sources and updates

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