TARGET M0035472040Recalls & reported problems
Stryker Corporation · 360 Soft Detachable Coil · Class 2 · Implant
All models of TARGET (114)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613252192701), received between Jun 12, 2018 and Jun 16, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Premature Separation” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Premature Separation1
Patient problems
- Aneurysm1
- No Clinical Signs, Symptoms or Conditions1
- Rupture1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 16, 2026Premature Separation
IT WAS REPORTED DURING THE PROCEDURE WHEN THE SUBJECT COIL WAS BEING DELIVERED IN ANEURYSM, IT PREMATURELY DETACHED. A STENT RETRIEVER AND SNARE WERE USED TO RETRIEVE THE DETACHED COIL BUT WERE UNSUCCESSFUL. THE PHYSICIAN USED AN ASPIRATION CATHETER AND SNARE TO REMOVE THE COIL SUCCESSFULLY WITHOUT COMPROMISING THE ANEURYSM. THE PROCEDURE WAS COMPLETED. NO OTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25518155 ↗InjuryJun 12, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT DURING A COIL EMBOLIZATION PROCEDURE, THE COIL (SUBJECT DEVICE) RUPTURED THE ANEURYSM. THE PATIENT WAS TREATED WITH A VENTRICULAR SHUNT. THE PHYSICIAN STATED THAT THE PROCEDURAL COMPLICATIONS WERE NOT RELATED TO THE STRYKER COIL. THERE IS NO FURTHER INFORMATION AVAILABLE.
Patient problems: Aneurysm; Rupture
MAUDE report 7594827 ↗
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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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