EVOS 72468107NRecalls & reported problems
Smith & Nephew, Inc. · EVOS DISTAL RADIUS VOLAR PLATE 7 HOLE LEFT STANDARD 100MM · Class 2 · Implant
All models of EVOS (190)
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 00885556713624), received between Apr 28, 2022 and Apr 28, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Defective Device” (1 report).
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.
Most reported problems
Device problems
- Defective Device1
Patient problems
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 28, 2022Defective Device; Defective Device
IT WAS REPORTED THAT, DURING AN INTERNAL FIXATION SURGERY, THE SURGEON ATTEMPTED TO INSERT A LOCKING SCREW PERPENDICULAR TO THE EVOS DISTAL RADIUS VOLAR PLATE 7 HOLE LEFT STANDARD 100MM BUT IT DID NOT LOCK, IT KEPT SPINNING. THE LOCKING SCREW WAS REMOVED AND ANOTHER SCREW ATTEMPTED INTO THE SAME SCREW HOLE AND IT WENT THROUGH THE PLATE. ANOTHER LOCKING SCREW WAS PLACED IN AN ADJACENT SCREW HOLE. SURGERY WAS RESUMED, AFTER A NON-SIGNIFICANT DELAY, WITH THE SAME DEVICE. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: Perforation
MAUDE report 14246937 ↗
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- 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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