EVOS 72413542Recalls & reported problems
Smith & Nephew, Inc. · EVOS 3.5MM X 42MM LOCKING SCREW SELF-TAPPING · 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 00885556637067), received between Oct 13, 2020 and Oct 13, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (1 report).
1 other recall cover devices cleared under the same FDA submission (K162078, K210837, K213126); they may or may not involve this specific model.
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
- Inadequacy of Device Shape and/or Size1
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.
InjuryOct 13, 2020Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
IT WAS REPORTED THAT THE EVOS 3.5MM X 44MM LCK SCR S-T ((B)(4)) PACKAGE WAS LABELED AS A 44 MM BUT THE ACTUAL MEASURE IS 34 MM, THE EVOS 3.5MM X 42MM LCK SCR S-T ((B)(4)) PACKAGE WAS LABELED AS A 42 MM BUT THE ACTUAL MEASURE IS 28 MM AND THE EVOS 3.5MM X 24MM CTX SCR S-T ((B)(4) PACKAGE WAS LABELED AS A 24 MM BUT THE ACTUAL MEASURE IS 30 MM. THE ACTION TAKEN WAS TO RE-MEASURED SCREWS BEFORE HANDING TO SURGEON BEFORE INSERTION, SO SURGEON REMOVED THE ABOVE SCREWS AND DRILLED AGAIN DUE TO ADJUSTMENT WITH PLATES. SCREWS WERE MEASURED DIFFERENTLY TO ABOVE, HENCE USED DIFFERENT LENGTH EVOS SCREWS. SCREWS WERE DISCARDED AND ARE NOT AVAILABLE FOR EVALUATION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10675580 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K162078, K210837, K213126. One submission often covers many models, so check the product and lot details in each record.
- Z-0265-2022 · Oct 25, 2021 · Open, ClassifiedSmith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X 70MM. Sterile.
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- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- 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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