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PINNACLE 2217-60-005Recalls & reported problems

Depuy (Ireland) · PINNACLE IMPACTION INSTRUMENT TRAY · Class 1

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 10603295099208), received between Aug 17, 2020 and Aug 17, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Contamination /Decontamination Problem1

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.

  • MalfunctionAug 17, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem

    IT WAS REPORTED THAT A LOANER SET OF INSTRUMENTS WAS RECEIVED BACK FROM A HOSPITAL THAT CONTAINED RESIDUAL DEBRIS AND HAD TO BE RETURNED TO THE SITE FOR ADDITIONAL CLEANING BY THEIR STERILE PROCESSING DEPARTMENT.

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

    MAUDE report 10417406 ↗

Other TRAY, SURGICAL, INSTRUMENT devices

All TRAY, SURGICAL, INSTRUMENT devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.