TARGET M0035467150Recalls & reported problems
Stryker Corporation · 360 Standard Detachable Coil · Class 2 · Implant
Data updated Oct 13, 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 07613252192602), received between Jun 20, 2022 and Jun 20, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Expulsion” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Expulsion1
- Premature Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 20, 2022Expulsion; Premature Separation; Expulsion; Premature Separation
IT WAS REPORTED THAT DURING PROCEDURE THE COIL (SUBJECT DEVICE) PREMATURELY DETACHED. THE COIL (SUBJECT DEVICE) WAS NOT COMPLETELY INSIDE THE ANEURYSM. SEVERAL STENTS RETRIEVERS AND A SNARE WERE USED AS A MEDICAL INTERVENTION TO RETRIEVE THE COIL (SUBJECT DEVICE). THE PATIENT NEEDED MEDICATION TO PREVENT ANY CLOT FORMING AROUND THE COIL (SUBJECT DEVICE). THE PROCEDURE HAD TO BE ABANDON AND THE PATIENT WILL COME BACK AGAIN FOR A NEW ATTEMPT. THE PATIENT WOKE UP WITHOUT ANY DEFICITS. NO CLINICAL CONSEQUENCES WERE REPORTED TO THE PATIENT DUE TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14748362 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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