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
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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- NA 532.021Synthes GmbH · INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT521 reports
- NA 2570-04-501Depuy (Ireland) · INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT500 reports
- NA 532.110Synthes GmbH · INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT433 reports
- NA 05.001.223Synthes GmbH · INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT397 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.
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