EVOS 71174906Recalls & reported problems
Smith & Nephew, Inc. · 1.8MM DRILL LONG WITH AO QUICK CONNECT · Class 1
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00885556386590), received between Sep 6, 2018 and Mar 18, 2026 — classified as 3 injuries, 1 malfunction.
The most frequently reported specific device problem is “Break” (2 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.
Reports received per month
Most reported problems
Device problems
- Break2
- Fracture1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Device Embedded In Tissue or Plaque1
- Foreign Body In Patient1
- Injury1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMar 18, 2026Fracture
IT WAS REPORTED THAT DURING THE PELVIC OSTEOSYNTHESIS PROCEDURE, THE 1.8MM DRILL LONG W/AO QC BIT BROKE WHILE DRILLING, LEAVING A FRAGMENT INSIDE THE BONE. THE PROCEDURE WAS RESUMED, WITHOUT ANY DELAY, USING AN EQUIVALENT S+N BACK-UP DEVICE. PATIENT WAS NOT INJURED AS CONSEQUENCE OF THIS PROBLEM.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 24626470 ↗InjurySep 1, 2021Break; Break
IT WAS REPORTED THAT, DURING AN ORIF OF THE CLAVICLE AND SCAPULA, THE TIP OF A 1.8MM DRILL LONG W/AO QC BROKE IN THE SCAPULA. THE BROKEN PIECE WAS UNREMOVABLE. THE SURGEON DECIDED TO LEAVE THE BROKEN PIECE IN THE PATIENT BECAUSE IT WOULD HAVE BEEN MORE INVASIVE TO REMOVE AND IT DOESN¿T CAUSE THE PATIENT ANY HARM LEAVING IN. THE PROCEDURE WAS COMPLETED, WITH A DELAY LESS THAN 30 MIN, USING A S+N BACK-UP DEVICE. THE CONDITION OF THE PATIENT IS GOOD.
Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions
MAUDE report 12410904 ↗MalfunctionFeb 9, 2021Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT, DURING AN UNKNOWN PROCEDURE, THE DRILL GOT BOUND IN THE DRILL GUIDE AND SNAPPED OFF. INSTRUMENTS WERE OUTSIDE THE PATIENT. THERE WAS NO DELAY AND THE PROCEDURE WAS FINISHED WITH A SMITH AND NEPHEW BACK UP DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11300206 ↗InjurySep 6, 2018Break; Break
IT WAS REPORTED THAT DURING OPERATION, DRILL BIT WAS IN USE AND BROKE INSIDE THE BONE AND WAS LEFT IN THE PLACE.
Patient problems: Injury
MAUDE report 7851472 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.