PROFYLE 60-25126Recalls & reported problems
Stryker GmbH · Drill, WL 59mm, Stryker-Shaft · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04546540247360), received between Nov 18, 2022 and Nov 21, 2022 — classified as 3 injuries.
The most frequently reported specific device problem is “Use of Device 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.
Most reported problems
Device problems
- Use of Device Problem3
Patient problems
- Perforation3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryNov 21, 2022Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT "TOO FAST THREADED DRILL (SECOND DEVICE), FOR WHICH THE SURGEON PIERCED THE FINGER OF THE PATIENT. INJURIES REQUIRING HEALING CARE."
Patient problems: Perforation
MAUDE report 15840844 ↗InjuryNov 21, 2022Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT "TOO FAST THREADED DRILL (SECOND DEVICE), FOR WHICH THE SURGEON PIERCED THE FINGER OF THE PATIENT. INJURIES REQUIRING HEALING CARE."
Patient problems: Perforation
MAUDE report 15840698 ↗InjuryNov 18, 2022Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT "TOO FAST THREADED DRILL (SECOND DEVICE), FOR WHICH THE SURGEON PIERCED THE FINGER OF THE PATIENT. INJURIES REQUIRING HEALING CARE."
Patient problems: Perforation
MAUDE report 15829361 ↗
Other BIT, DRILL devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 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