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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 1 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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

All BIT, DRILL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.