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VLP MINI-MOD 74461500Recalls & reported problems

Smith & Nephew, Inc. · VLP MINI-MOD 1.1MM DRILL MINI QUICK CONNECT · Class 1

All models of VLP MINI-MOD (22)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885556484296), received between May 10, 2021 and Nov 13, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Material Twisted/Bent” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 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

  • Material Twisted/Bent2
  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • Insufficient Information1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 13, 2025Fracture; Fracture

    IT WAS REPORTED THAT DURING AN OSTEOSYNTHESIS SURGERY, WHEN DRILLING, ONE (1) 1.1/1.5 DOUBLE DRILL GUIDE BREAKS, THE PIECE FELL INTO THE PATIENT'S WOUND, THAT PART OF THE DRILL WAS REMOVED WITH A "NELLY", ALL PIECES REMOVED AND ACCOUNTED. THE PROCEDURE WAS COMPLETED, AFTER A NON-SIGNIFICANT DELAY, USING A SIMILAR S+N BACKUP PRODUCT. NO INJURY WAS REPORTED AS A CONSEQUENCE OF THIS ISSUE.

    Patient problems: Insufficient Information

    MAUDE report 23544482 ↗
  • MalfunctionMay 10, 2021Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED THAT, DURING A TRAUMA SURGERY, TWO (2) VLP MINI-MOD 1.1MM DRILL MINI QC WERE BENT. THE INSTRUMENTS WERE OUTSIDE OF THE PATIENT. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT DELAY USING A SMITH AND NEPHEW BACK UP DEVICE. PATIENT WAS NOT HARMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11803374 ↗
  • MalfunctionMay 10, 2021Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED THAT, DURING A TRAUMA SURGERY, TWO (2) VLP MINI-MOD 1.1MM DRILL MINI QC WERE BENT. THE INSTRUMENTS WERE OUTSIDE OF THE PATIENT. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT DELAY USING A SMITH AND NEPHEW BACK UP DEVICE. PATIENT WAS NOT HARMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11803252 ↗

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Sources and updates

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