EVOS 72466304Recalls & reported problems
Smith & Nephew, Inc. · EVOS 2.7MM/3.5MM OLECRANON PLATE WITH TINES 4 HOLE LEFT 82MM · 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 00885556665046), received between Jun 26, 2020 and Jun 26, 2020 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 26, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE EVOS 2.7MM/3.5MM OLECRANON PLATE WITH TINES 4H L 82MM WAS IMPLANTED IN THE RIGHT ARM OF THE PATIENT AND LATER IT WAS FOUND OUT THAT THE DEVICE WAS INTENDED FOR THE LEFT SIDE. THE PATIENT IS IN GOOD HEALTH AND HAS NOT EXPERIENCED ANY PROBLEMS. THE LABELING OF THE DEVICE WAS NOT INCORRECT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10203465 ↗
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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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