QUICKSET 2274-47-000Recalls & reported problems
Depuy (Ireland) · QUICKSET TAPERED HEX SCREWDRIVER RIGID · Class 1
All models of QUICKSET (66)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This DePuy QuickSet screwdriver is a hand tool used to drive screws during orthopedic surgery. Many of its 487 reports describe tips that are worn down, bent or deformed, and some describe broken instruments. Most patients had no consequences, and the reports include 1 injury and no deaths. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 487
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 487 adverse event reports that list this exact device (DI 10603295109235), received between Jun 29, 2017 and Jun 27, 2025 — classified as 1 injury, 486 malfunctions.
The most frequently reported specific device problem is “Naturally Worn” (197 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.
Reports received per month
Most reported problems
Device problems
- Naturally Worn197
- Material Twisted/Bent147
- Material Deformation92
- Appropriate Device Problem Term/Code Not Available48
- Break40
- Device-Device Incompatibility38
- Dull, Blunt19
- Adverse Event Without Identified Device or Use Problem10
Patient problems
- No Consequences Or Impact To Patient255
- No Clinical Signs, Symptoms or Conditions181
- No Information44
- Insufficient Information19
- Not Applicable10
- No Code Available6
Recent adverse event reports
The 25 most recent of 487 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 27, 2025Break; Break
IT WAS REPORTED THAT THE INSTRUMENTS WERE BROKEN. IT DID NOT HAPPEN IN SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22350069 ↗MalfunctionMay 8, 2025Break; Device-Device Incompatibility; Break; Device-Device Incompatibility
IT WAS REPORTED THAT THERE WAS A BROKEN INSTRUMENT. THE SCREWDRIVER, ONCE IN THE SCREW HEAD, WAS VERY DIFFICULT TO SEPARATE ONCE THE SCREW WAS IMPLANTED.
Patient problems: Insufficient Information
MAUDE report 21984753 ↗MalfunctionJan 9, 2025Break; Device-Device Incompatibility; Material Deformation; Break; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THE SCREW DRIVER TIP WAS NOT HOLDING THE SCREW WELL AND THE TIP HAS CROSSED THREADS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21114877 ↗MalfunctionDec 10, 2024Device-Device Incompatibility; Material Deformation; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT THE STRAIGHT SCREW INSERTER SHAFT WAS WORN AT THE TIP AND WOULD NOT THREAD THE TRIAL LINER.
Patient problems: Insufficient Information
MAUDE report 20893154 ↗MalfunctionJun 1, 2024Break; Break
IT WAS REPORTED THAT TIP OF SCREWDRIVER WAS BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19442729 ↗MalfunctionApr 18, 2024Break; Material Deformation; Break; Material Deformation
IT WAS REPORTED THAT THE TIP ON DRIVER IS BEGINNING TO WARP. IT NEEDS REPLACEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19133810 ↗MalfunctionJan 26, 2024Break; Naturally Worn; Break; Naturally Worn
ADDITIONAL INFORMATION RECEIVED STATES THAT THERE HAS BEEN NO HARM TO PATIENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18590204 ↗MalfunctionSep 28, 2023Break; Break
IT WAS REPORTED THAT THE DEVICE HAS BROKEN. NO IMPACT TO PATIENT OR SURGERY TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17836410 ↗MalfunctionJul 14, 2023Break; Break
IT WAS REPORTED THAT SCREWDRIVER BROKE . SURGICAL DELAY UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17327634 ↗MalfunctionJun 6, 2023Break; Break
IT WAS REPORTED THAT THE HEX DRIVER WAS TORN UP DURING THE CASE WHILE REMOVING SCREWS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17071614 ↗MalfunctionJun 6, 2023Break; Break
IT WAS REPORTED THAT THE HEX DRIVER WAS TORN UP DURING THE CASE WHILE REMOVING SCREWS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17071611 ↗MalfunctionMay 15, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE STRAIGHT PINNACLE DRIVER SHAFT IS WORN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16930857 ↗MalfunctionMay 15, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE HEAD OF SCREWDRIVER IS STRIPPED FROM OVERUSE. ANOTHER DRIVER WAS USED. THERE WAS NO DELAY IN CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16930694 ↗MalfunctionMay 5, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT DURING SURGERY THE SURGEON WAS PLACING SCREWS INTO THE ACETABULUM. WHILE DOING SO, THE STRAIGHT SCREWDRIVER END STRIPPED AND WAS NOT ABLE TO CONTINUE WITH THE STRAIGHT SCREWDRIVER ATTACHMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16879939 ↗MalfunctionApr 25, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE INSTRUMENTS ARE WORN DUE TO FAIR WEAR AND TEAR. SURGICAL DELAY OF 5 MINUTES OCCURRED. NO ADVERSE AFFECTS ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16811431 ↗MalfunctionApr 20, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SCREWDRIVER BLADE WAS BEGINNING TO STRIP SCREWS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16776413 ↗MalfunctionApr 12, 2023Naturally Worn; Illegible Information; Naturally Worn; Illegible Information
IT WAS REPORTED THAT THE HEX TIP OVER SCREW DRIVER SHAFT IS VERY WORN DOWN/STRIPPED DUE TO USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16725769 ↗MalfunctionApr 4, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE RIGID SCREWDRIVER WAS STRIPPED. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16672938 ↗MalfunctionMar 30, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT IT WAS DISCOVERED THAT ONE OF THE SCREWDRIVER TIPS ARE BAD AND NEED REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16652086 ↗MalfunctionMar 28, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE HEX DRIVER WAS STRIPPED AND ROUNDED OFF. THERE WAS NOTHING LEFT IN THE PATIENT. THERE WAS NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16632825 ↗MalfunctionMar 28, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SURGEON WAS USING DRIVER TO IMPLANT HOLE ELIMINATOR . HE COMPLAINED THE DRIVER IS STRIPED. THERE WAS NO ISSUE IMPLANTING THE HOLE ELIMINATOR. SURGERY WAS NOT DELAYED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16627464 ↗MalfunctionMar 21, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SCREWDRIVER TIP WAS STRIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16581378 ↗MalfunctionMar 17, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE SCREWDRIVER SHAFT IS STRIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16563433 ↗MalfunctionMar 14, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
IT WAS REPORTED THAT THE SCREWDRIVER TIP IS STRIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16538462 ↗MalfunctionMar 13, 2023Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE QUICKSET TAPER HEX SCDR RIGID AND QUICKSET TPRD HEX SCDR U-JOINT BOTH DEVELOPED ROUNDED HEAD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16529135 ↗
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
- NA 03.130.010Synthes GmbH · SCREWDRIVER1 recall422 reports
- QUICKSET 2274-63-000Depuy (Ireland) · SCREWDRIVER404 reports
- EVOS 71175072Smith & Nephew, Inc. · SCREWDRIVER336 reports
- NA 2274-02-000Depuy (Ireland) · SCREWDRIVER303 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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