EVOS 72585120Recalls & reported problems
Smith & Nephew, Inc. · EVOS 3.5MM/4.5MM PERIPROSTHETIC DISTAL FEMUR SPAN PLATE L 20H 405MM · 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 00885556771082), received between Jan 19, 2024 and Jan 19, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 19, 2024Fracture; Fracture
IT WAS REPORTED THAT, THE PATIENT UNDERWENT AN INTERNAL FIXATION SURGERY IN OR ABOUT (B)(6) 2022, IN WHICH IN THE LEFT LEG AN UNSPECIFIED SMITH AND NEPHEW TRAUMA ORTHO DEVICE WAS IMPLANTED. WITHIN SIX MONTHS POST OPERATION, THE PATIENT EXPERIENCED A BREAKAGE OF THE DEVICE. THIS COMPLICATION WAS SOLVED BY CONDUCTING A REVISION SURGERY ON AN UNKNOWN DATE IN WHICH THE BROKEN DEVICE WAS REMOVED. CURRENT HEALTH STATUS OF THE PATIENT AND ADDITIONAL INFORMATION ARE UNKNOWN.
Patient problems: Failure of Implant
MAUDE report 18544212 ↗
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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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