Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GDC-10 360 SOFT 3mm x 6cm SR Recalled by Stryker Neurovascular Due to Units of GDC 360 coils, Target coil and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Neurovascular directly.
Affected Products
GDC-10 360 SOFT 3mm x 6cm SR ; GDC 360¿ Detachable Coils are intended for embolization of those intracranial aneurysms that- because of their morphology, their location, or the patient 's general medical condition - are considered by the treating neurosurgical team to be a) very high risk for management by traditional operative techniques, or b) inoperable
Quantity: 1
Why Was This Recalled?
Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were shipped to US customers beyond the expiration date.
Where Was This Sold?
This product was distributed to 4 states: NH, OH, TX, VA
About Stryker Neurovascular
Stryker Neurovascular has 108 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report