EVOS 71177726Recalls & reported problems
Smith & Nephew, Inc. · EVOS LARGE TARGETER 3.5MM PROVISIONAL FIXATION PIN 40MM · Class 1
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 00885556767641), received between Mar 24, 2025 and Mar 24, 2025 — 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
- 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.
InjuryMar 24, 2025Fracture; Fracture
IT WAS REPORTED THAT, DURING A LEFT LATERAL DISTAL FEMORAL PERI-PROSTHETIC FRACTURE CASE, THE EVOS LARGE TGTR 3.5MM PF PIN 40MM WAS USED TO REDUCE THE PLATE DOWN TO THE PROXIMAL FEMORAL BONE. WHILE DRILLING THE EVOS LARGE TGTR 3.5MM PF PIN 40MM INTO THE BONE, THE THREADED TIP SEVERED AND BROKE IN THE BONE. THERE WAS A NON-SIGNIFICANT DELAY AND THE PROCEDURE WAS FINISHED USING A SMITH & NEPHEW BACK UP. NO FURTHER COMPLICATIONS WERE REPORTED AS A CONSEQUENCE OF THIS PROBLEM.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 21679249 ↗
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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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