Euroscrew TCP NG Ø9 L24Recalls & reported problems
Teknimed · Class 2 · Implant
Data updated Oct 18, 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 03760177042827), received between Nov 22, 2024 and Nov 22, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Migration or Expulsion of Device” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Migration or Expulsion of Device1
Patient problems
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 22, 2024Migration or Expulsion of Device; Migration or Expulsion of Device
A PATIENT OPERATED ON HER KNEE TIBIA FOR ACL SURGERY ON (B)(6) 2022 HAS COMPLAINED OF DISCOMFORT IN THE KNEE. AFTER CHECKING IT, TURNED OUT THAT THE SCREW INSTALLED AT THE TIME HAD BROKEN IN TWO WITH THE HEAD WHICH HAD GONE UP INTO THE KNEE (INTRA-ARTICULAR TIBIAL MIGRATION POST INITIAL SURGERY). AN ADDITIONAL SURGICAL INTERVENTION HAS BEEN PERFORMED TO EXTRACT THE SCREW ON (B)(6) 2024. AFTER THE ADDITIONAL SURGICAL INTERVENTION, THE PATIENT IS DOING WELL.
Patient problems: Implant Pain
MAUDE report 20758680 ↗
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- HEALICOIL 72205137Smith & Nephew, Inc. · Fastener, fixation, biodegradable, soft tissue427 reports
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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