Target Tetra TG5414510Recalls & reported problems
Stryker Corporation · Detachable Coil · Class 2 · Implant
All models of Target Tetra (19)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327578744), received between Sep 2, 2025 and May 21, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Premature Separation” (2 reports).
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
- Premature Separation2
- Failure to Advance1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2026Premature Separation
IT WAS REPORTED THAT DURING A COILING PROCEDURE, THE COIL WAS PARTIALLY DEPLOYED BY THE PHYSICIAN, THE PHYSICIAN WANTED TO REDEPLOY THE SUBJECT COIL AS SOME LOOPS WERE COMING OUTSIDE. IN THE PROCESS THE SUBJECT COIL GOT STUCK IN THE MICROCATHETER AND THERE WAS RESISTANCE IN THE MICROCATHETER. THE SUBJECT COIL GOT STUCK IN THE MICROCATHETER AND IT GOT SELF-DETACHED WITHIN THE MICROCATHETER. THE SUBJECT DEVICE WAS REPLACED, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO CLINICAL CONSEQUENCES WERE REPORTED TO THE PATIENT DUE TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25247870 ↗MalfunctionMar 20, 2026Premature Separation
IT WAS REPORTED THAT THE SUBJECT COIL WAS DEPLOYED PREMATURELY INSIDE THE PATIENT. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO CLINICAL CONSEQUENCES WERE REPORTED TO THE PATIENT DUE TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24651559 ↗MalfunctionSep 2, 2025Failure to Advance
FROM STAFF: USING COILS DURING EMBOLIZATION FOR NEURO COIL UNABLE TO BE PUSHED THROUGH MICROCATH. COIL WAS 4.5X10 TARGET TETRA COIL.
Patient problems: Insufficient Information
MAUDE report 22929653 ↗
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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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