QUICKSET 2440-00-503Recalls & reported problems
Depuy (Ireland) · QUICKSET ACETABULAR GRATER CASE BASE · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295123736), received between May 12, 2022 and Sep 8, 2023 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (8 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Contamination /Decontamination Problem8
- Peeled/Delaminated7
- Break1
- Corroded1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 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 17712491 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14372953 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14372874 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT THE TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14371028 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT THE TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14371022 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT THE TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14370999 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT THE TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14370911 ↗MalfunctionMay 12, 2022Peeled/Delaminated; Contamination /Decontamination Problem; Peeled/Delaminated; Contamination /Decontamination Problem
IT WAS REPORTED THAT THE TRAYS ARE BEING REJECTED BY THE HOSPITAL DUE TO STAINING AND BURNING OF THE ALUMINUM CASKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14370863 ↗
Other TRAY, SURGICAL, INSTRUMENT devices
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- ATTUNE 2545-01-703Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT62 reports
- ATTUNE 2545-01-704Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT57 reports
- INSTRUMENT 6541-9-109Howmedica Osteonics Corp. · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- Medical Action Industries 6805Medical Action Industries Inc. · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 39501CECKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
- n.a. 11580AKarl Storz GmbH & Co. KG · TRAY, SURGICAL, INSTRUMENT1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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