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PINNACLE 2218-90-048Recalls & reported problems

Depuy (Ireland) · PINNACLE GRIPPER 48mm · Class 1

All models of PINNACLE (198)

Data updated Oct 16, 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 10603295102267), received between May 24, 2021 and Apr 4, 2023 — 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 16, 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.

  • MalfunctionApr 4, 2023Break; Break

    IT WAS REPORTER THE INSERTION DEVICE BROKE DURING LINER INSERTION. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16672481 ↗
  • MalfunctionMay 24, 2021Break; Break

    REAMER SEPARATED INTO 2 PIECES, THE BOTTOM DETACHED, ALL PIECES WERE RECOVERED, NO FURTHER INFO AVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11870252 ↗

Other WRENCH devices

All WRENCH devices →

Sources and updates

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