VLP MINI-MOD 74412424Recalls & reported problems
Smith & Nephew, Inc. · VLP TITANIUM 2.4MM X 24MM LOCKING SCREW T7 SELF-TAPPING · Class 2 · Implant
All models of VLP MINI-MOD (22)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556349045), received between Jul 8, 2025 and Jul 8, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Positioning Problem” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K132886, K210837, K213126); they may or may not involve this specific model.
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
- Positioning Problem1
Patient problems
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 8, 2025Positioning Problem; Positioning Problem
IT WAS REPORTED THAT, DURING INTERNAL FIXATION SURGERY OF RADIUS FRACTURE, THE PROXIMAL RADIAL VLP TI 2.4MM X 24MM LCK SCR T7 S-T PASSED THROUGH THE EVOS VOLAR PLATE 3H LEFT WDE TI 48MM AND DID NOT ENGAGE WITH IT. THE SCREW COULD NOT BE REMOVED, THEREFORE HAD TO BE LEFT IN SITU. NO PROCEDURE HAS BEEN SCHEDULED FOR REMOVAL. IT HAD GOOD FIXATION; THE SURGEON WAS SATISFIED WITH THE OUTCOME OF THE SURGERY. IN ADDITION, NO PHYSICAL DAMAGE TO EITHER THE SCREW OR THE PLATE WAS OBSERVED. THE PROCEDURE WAS RESUMED, AFTER A NON-SIGNIFICANT DELAY, WITH THE SAME DEVICE. THE PATIENT HAS BEEN DISCHARGED FROM HOSPITAL. NO INJURY WAS REPORTED AS A CONSEQUENCE OF THIS ISSUE.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 22439188 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K132886, K210837, K213126. One submission often covers many models, so check the product and lot details in each record.
- Z-0396-2018 · Dec 11, 2017 · Terminatedsmith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STRAIGHT PLATE, 8 HOLE VLP(R) MIN-MOD, REF 74442024, QTY: (
- Z-0397-2018 · Dec 11, 2017 · Terminatedsmith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STOUT STRAIGHT PLATE, 8 HOLE VLP(R) MIN-MOD, REF 74442030,
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 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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