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QUICKSET 2440-00-502Recalls & reported problems

Depuy (Ireland) · QUICKSET ACETABULAR GRATER CASE LID · 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 10603295123729), received between Sep 8, 2023 and Sep 8, 2023 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1
  • Contamination /Decontamination Problem1
  • Corroded1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 8, 2023Break; Corroded; Contamination /Decontamination Problem; Break; Corroded; Contamination /Decontamination Problem

    THE PTA INSTRUMENT WAS RECEIVED AT THE CENTRAL STERILIZATION SERVICE, DURING THE TRACEABILITY PROCESS, IT WAS VERIFIED THAT THE STATUS OF THE TRAYS AND LID WAS ALREADY DETERIORATED: LID AND BROKEN TRAYS, WITH HOLES AND GLUE, OXIDIZED MILLS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17712382 ↗

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.