QUICKSET 2274-50-000Recalls & reported problems
Depuy (Ireland) · QUICKSET SCREWDRIVER, CROSS HEAD · Class 1
All models of QUICKSET (66)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295109266), received between Mar 23, 2018 and Sep 13, 2021 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Naturally Worn” (4 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Naturally Worn4
- Device Issue1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient2
- No Code Available1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 13, 2021Naturally Worn; Naturally Worn
IT WAS REPORTED THAT WHILE CHECKING IN A PINNACLE SCREW SET, IT WAS DISCOVERED THAT THE CROSS HEAD SCREWDRIVER ONLY HAD 2 ROUNDED SIDES INSTEAD OF 4 ROUNDED SIDES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12459363 ↗MalfunctionSep 13, 2021Naturally Worn; Naturally Worn
IT WAS REPORTED THAT WHILE CHECKING IN A PINNACLE SCREW SET, IT WAS DISCOVERED THAT THE CROSS HEAD SCREWDRIVER ONLY HAD 2 ROUNDED SIDES INSTEAD OF 4 ROUNDED SIDES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12459360 ↗MalfunctionJan 4, 2019Naturally Worn; Naturally Worn
THE DRILL BIT ON THE FLEXIBLE ONE PIECE DRILL BIT SNAPPED DURING USE, THE SCREW DRIVERS WERE ALL REPORTED BY THE SURGEON TO BE DAMAGED. THE RATCHET HANDLE WAS JAMMED AND UNABLE TO BE USED AS DESIGNED.
Patient problems: No Code Available
MAUDE report 8219181 ↗MalfunctionOct 11, 2018Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SCREWDRIVER STRIPPED OUT DURING SURGERY, WON'T TURN SCREW.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7958006 ↗MalfunctionMar 23, 2018Device Issue; Device Issue
FLEXIBLE DRILL SHAFT NOT HOLDING DRILL BIT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7366644 ↗
Other SCREWDRIVER devices
- DELTA XTEND 2307-92-003Depuy (Ireland) · SCREWDRIVER751 reports
- EXPEDIUM 279712400Medos International Sàrl · SCREWDRIVER551 reports
- NA 314.467Synthes GmbH · SCREWDRIVER498 reports
- N/A 5584111Medtronic Sofamor Danek, Inc. · SCREWDRIVER492 reports
- QUICKSET 2274-47-000Depuy (Ireland) · SCREWDRIVER487 reports
- NA 03.130.010Synthes GmbH · SCREWDRIVER1 recall422 reports
- QUICKSET 2274-63-000Depuy (Ireland) · SCREWDRIVER404 reports
- EVOS 71175072Smith & Nephew, Inc. · SCREWDRIVER336 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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