Skip to content

PINNACLE 2218-90-064Recalls & reported problems

Depuy (Ireland) · PINNACLE GRIPPER 64mm · Class 1

All models of PINNACLE (198)

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 10603295102342), received between Nov 7, 2018 and Nov 7, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

  • Component Missing1

Patient problems

  • Not Applicable1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 7, 2018Component Missing; Component Missing

    TWO OF THE TABS WERE MISSING.

    Patient problems: Not Applicable

    MAUDE report 8048270 ↗

Other WRENCH devices

All WRENCH devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page