QUICKSET 2440-00-505Recalls & reported problems
Depuy (Ireland) · QUICKSET ACETABULAR GRATER CASE MIDDLE TRAY · Class 1
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295123750), received between Oct 9, 2018 and Oct 3, 2023 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (3 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.
Reports received per month
Most reported problems
Device problems
- Contamination /Decontamination Problem3
- Corroded3
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 3, 2023Corroded; Contamination /Decontamination Problem; Corroded; Contamination /Decontamination Problem
THE DEVICE DAMAGED FOLLOWING THE CLEANING PROCESS AT THE FACILITY: THEY GOT RUSTED. AFTER SEVERAL CLEANINGS, THE RUST/DIRT ON THE PRODUCTS DOES NOT REMOVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17859868 ↗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 17712711 ↗MalfunctionNov 13, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem
IT WAS REPORTED THAT ALL THREE INNER TRAYS OF THE PINNACLE GREATER INSTRUMENT SET ARE STAINED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10839651 ↗MalfunctionOct 9, 2018Corroded; Corroded
IT WAS REPORTED THAT THE PINNACLE SCREW CADDY APPEARS STAINED AND UNABLE TO CLEAN PROPERLY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7947920 ↗
Other TRAY, SURGICAL, INSTRUMENT devices
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- ACTIS 2010-04-200Depuy (Ireland) · TRAY, SURGICAL, INSTRUMENT66 reports
- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.