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VLP MINI-MOD 74412415Recalls & reported problems

Smith & Nephew, Inc. · VLP TITANIUM 2.4MM X 15MM 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556348598), received between Feb 10, 2026 and Feb 10, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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

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: 1 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

  • Migration1

Patient problems

  • Insufficient Information1
  • Loss of fracture reduction1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 10, 2026Migration

    IT WAS REPORTED THAT, AFTER A PRIMARY TRAUMA SURGERY HAD BEEN PERFORMED ON (B)(6) 2025, TO TREAT A DISTAL RADIUS FRACTURE USING EVOS PLATE AND SCREWS, THE PATIENT EXPERIENCED FLOATING/LOOSENING OF THE EVOS VOLAR PLATE 4H LEFT STD TI 56MM. ON (B)(6) 2026, AN X-RAY REVEALED A SCREW BACK OUT. THIS ADVERSE EVENT WAS SOLVED BY REVISION TRAUMA SURGERY ON (B)(6) 2026, IN WHICH THE COMPLAINT DEVICES WERE CONFIRMED; THE MOST PROXIMAL LOCKING SCREW HAD BEEN PASSED THE SCREW HOLE ON THE PLATE. BOTH DEVICES WERE EXPLANTED. PATIENT'S CURRENT HEALTH STATUS IS UNKNOWN. NO FURTHER COMPLICATIONS WERE REPORTED.

    Patient problems: Insufficient Information; Loss of fracture reduction

    MAUDE report 24310439 ↗

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 · Terminated
    smith&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 · Terminated
    smith&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,

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page