QUICKSETRecalls & reported problems across all models
Depuy (Ireland) · 66 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 21,038
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls
- 0
We found 66 models of QUICKSET by Depuy (Ireland) in the FDA's device registry (GUDID). Together they are named in 21,038 adverse event reports in the FDA's MAUDE database, received between Jun 28, 2017 and Sep 29, 2026 — classified as 9 injuries, 21,029 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (13,377 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported QUICKSET problems
Device problems
- Failure to Cut13,377
- Naturally Worn2,431
- Dull, Blunt2,249
- Break1,479
- Corroded1,471
- No Apparent Adverse Event990
- Material Twisted/Bent694
- Material Deformation472
Patient problems
- No Clinical Signs, Symptoms or Conditions15,889
- No Consequences Or Impact To Patient3,789
- Insufficient Information1,086
- No Information492
- No Code Available261
- Not Applicable172
- No Known Impact Or Consequence To Patient11
- Foreign Body In Patient8
QUICKSET models
66 models, most reported first. Each model has its own page with its reports, recalls and device details.
- QUICKSET 2440-00-551REAMER1,150 reports
- QUICKSET 2440-00-549REAMER1,113 reports
- QUICKSET 2440-00-553REAMER1,105 reports
- QUICKSET 2440-00-547REAMER1,073 reports
- QUICKSET 2440-00-555REAMER1,065 reports
- QUICKSET 2440-00-557REAMER1,031 reports
- QUICKSET 2440-00-545REAMER947 reports
- QUICKSET 2440-00-552REAMER888 reports
- QUICKSET 2440-00-550REAMER870 reports
- QUICKSET 2440-00-548REAMER857 reports
- QUICKSET 2440-00-554REAMER840 reports
- QUICKSET 2440-00-556REAMER817 reports
- QUICKSET 2440-00-546REAMER754 reports
- QUICKSET 2440-00-559REAMER696 reports
- QUICKSET 2440-00-558REAMER655 reports
- QUICKSET 2440-00-544REAMER568 reports
- QUICKSET 2440-00-543REAMER557 reports
- QUICKSET 2274-47-000SCREWDRIVER487 reports
- QUICKSET 2440-00-560REAMER457 reports
- QUICKSET 2440-00-561REAMER418 reports
- QUICKSET 2274-63-000SCREWDRIVER404 reports
- QUICKSET 2440-00-510REAMER297 reports
- QUICKSET 2274-56-000BIT, DRILL275 reports
- QUICKSET 2440-00-562REAMER268 reports
- QUICKSET 2440-00-542REAMER267 reports
- QUICKSET 2440-00-563REAMER256 reports
- QUICKSET 2440-00-541REAMER250 reports
- QUICKSET 2440-00-540REAMER189 reports
- QUICKSET 2274-52-000BIT, DRILL186 reports
- QUICKSET 2440-00-564REAMER179 reports
- QUICKSET 2440-00-537REAMER171 reports
- QUICKSET 2440-00-539REAMER171 reports
- QUICKSET 2274-49-000SCREWDRIVER162 reports
- QUICKSET 2440-00-565REAMER159 reports
- QUICKSET 2440-00-536REAMER157 reports
- QUICKSET 2440-00-538REAMER157 reports
- QUICKSET 2440-00-566REAMER152 reports
- QUICKSET 2440-00-567REAMER120 reports
- QUICKSET 2274-57-000BIT, DRILL119 reports
- QUICKSET 2440-00-568REAMER110 reports
- QUICKSET 2274-58-000BIT, DRILL79 reports
- QUICKSET 2274-60-000GAUGE, DEPTH68 reports
- QUICKSET 2440-00-511ORTHOPEDIC MANUAL SURGICAL INSTRUMENT49 reports
- QUICKSET 2274-53-000BIT, DRILL41 reports
- QUICKSET 2440-00-569REAMER31 reports
- QUICKSET 2440-00-571REAMER28 reports
- QUICKSET 2440-00-570REAMER27 reports
- QUICKSET 2440-00-572REAMER27 reports
- QUICKSET 2440-00-573REAMER25 reports
- QUICKSET 2440-00-574REAMER25 reports
- QUICKSET 2440-00-501TRAY, SURGICAL, INSTRUMENT24 reports
- QUICKSET 2440-00-575REAMER23 reports
- QUICKSET 2440-00-576REAMER23 reports
- QUICKSET 2440-00-577REAMER23 reports
- QUICKSET 2440-00-579REAMER23 reports
- QUICKSET 2440-00-580REAMER23 reports
- QUICKSET 2440-00-578REAMER22 reports
- QUICKSET 2274-48-000SCREWDRIVER21 reports
- QUICKSET 2274-59-000BIT, DRILL18 reports
- QUICKSET 2274-55-000FORCEPS, GENERAL & PLASTIC SURGERY11 reports
- QUICKSET 2440-00-503TRAY, SURGICAL, INSTRUMENT8 reports
- QUICKSET 2274-64-000TRAY, SURGICAL, INSTRUMENT7 reports
- QUICKSET 2274-50-000SCREWDRIVER5 reports
- QUICKSET 2440-00-504TRAY, SURGICAL, INSTRUMENT5 reports
- QUICKSET 2440-00-505TRAY, SURGICAL, INSTRUMENT4 reports
- QUICKSET 2440-00-502TRAY, SURGICAL, INSTRUMENT1 report
Recent QUICKSET adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50928569 ↗MalfunctionSep 25, 2026Break
It was reported that reamer basket broke. There was no delay to the procedure. There were no adverse events. All parts were retrieved.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898514 ↗MalfunctionSep 18, 2026Mechanical Jam
It was reported that the grater device was too dull, the handles were too stiff, and the coating on the trays was peeling. The event did not occur during surgery. It was reported that during in-house engineering evaluation, it was determined that the device was deformed/bent. All available information has been disclosed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50819104 ↗MalfunctionSep 10, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50721851 ↗MalfunctionAug 13, 2026Break
A drill bit broke due to a mishap used during the procedure.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50240291 ↗MalfunctionAug 12, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50227819 ↗MalfunctionAug 7, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50174995 ↗MalfunctionAug 6, 2026Break; Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50164340 ↗MalfunctionAug 3, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50117667 ↗MalfunctionJul 30, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50086516 ↗MalfunctionJul 28, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50059487 ↗MalfunctionJul 27, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50045053 ↗MalfunctionJul 27, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50034644 ↗MalfunctionJun 30, 2026Device-Device Incompatibility
IT WAS REPORTED THAT THE SCREWDRIVER TIP WAS WORN AND WOULDN'T HOLD SCREW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25665914 ↗MalfunctionJun 25, 2026Break
IT WAS REPORTED THAT PRIOR TO SURGERY IT WAS OBSERVED THAT THE DRILL BITS WERE BROKEN. THERE WAS NO PATIENT CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25621123 ↗
Other Depuy (Ireland) products
All Depuy (Ireland) devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page