NA 2178-42-005Recalls & reported problems
Depuy Orthopaedics, Inc. · PATHWAY QUICK DRILL PIN DRIVER · Class 1
Data updated Oct 16, 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 10603295094869), received between Dec 6, 2018 and Aug 25, 2023 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device-Device Incompatibility8
- Naturally Worn7
Patient problems
- No Clinical Signs, Symptoms or Conditions7
- Not Applicable1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17628488 ↗MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17627608 ↗MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17627441 ↗MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17625447 ↗MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17625322 ↗MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17625166 ↗MalfunctionAug 25, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn
THE PW QDRILL PIN DRIVER NO LONGER GRIPS THE PINS PROPERLY. NO SPECIFIC LOT NUMBERS ARE AVAILABLE. THIS HAS NOT CAUSED SURGICAL DELAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17625097 ↗MalfunctionDec 6, 2018Device-Device Incompatibility; Device-Device Incompatibility
Other DRIVER, PROSTHESIS devices
- ATTUNE 2544-01-005Depuy (Ireland) · DRIVER, PROSTHESIS1,383 reports
- EXPEDIUM VERSE 299704230Medos International Sàrl · DRIVER, PROSTHESIS875 reports
- NA 9200-10-029Depuy (Ireland) · DRIVER, PROSTHESIS745 reports
- MOSS 279712600Depuy Spine, LLC · DRIVER, PROSTHESIS706 reports
- NA 2598-07-440Depuy (Ireland) · DRIVER, PROSTHESIS665 reports
- NA 2598-07-570Depuy (Ireland) · DRIVER, PROSTHESIS505 reports
- VIPER 286745550Depuy Spine, LLC · DRIVER, PROSTHESIS263 reports
- SUMMIT 2570-05-100Depuy (Ireland) · DRIVER, PROSTHESIS225 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 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