EVOS 72467305Recalls & reported problems
Smith & Nephew, Inc. · EVOS 2.7MM/3.5MM SUPERIOR DISTAL CLAVICLE PLATE 5 HOLE LEFT 89MM · 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 00885556665541), received between Oct 26, 2020 and Oct 26, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Connection Problem” (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
- Connection Problem1
- Loose or Intermittent Connection1
Patient problems
- Arthritis1
- Failure of Implant1
- Joint Laxity1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 26, 2020Loose or Intermittent Connection; Connection Problem; Loose or Intermittent Connection; Connection Problem
IT WAS REPORTED THAT THE PATIENT WAS OPERATED WITH THE EVOS CLAVICLE PLATE AND SCREWS, FOR AN PSEUDO ARTHROSIS, PATIENT HAD PAIN AFTER 14 DAYS, AND X-RAY REVEALED THAT ALL 5 LATERAL SCREWS (1 CORTEX AND 4 LOCKING), HAD LOOSENED AND LAY OUTSIDE THE PLATE AND JUST BENEATH THE SKIN. REVISION SURGERY WAS PERFORMED TO CORRECT THE PROBLEM.
Patient problems: Arthritis; Failure of Implant; Joint Laxity; Pain
MAUDE report 10737993 ↗
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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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