FDA Adverse Event Injury Summary report: N

UNKNOWN_NEUROVASCULAR_PRODUCT

MDR report key: 3372950 · Received September 27, 2013

Report

Report Number
3008853977-2013-00359
Event Type
Injury
Date Received
September 27, 2013
Date of Event
January 1, 2010
Report Date
September 23, 2013
Manufacturer
STRYKER NEUROVASCULAR CORK
Product Code
HCG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE REMAINS IMPLANTED AND WAS NOT AVAILABLE FOR ANALYSIS. FROM THE INFORMATION PROVIDED THERE WAS NO INDICATION THAT THE DEVICE WAS NOT USED AS IN ACCORDANCE WITH THE LABELING OR THAT THIS CAUSED OR CONTRIBUTED TO THE REPORTED EVENT. HEADACHE AND DIZZINESS ARE KNOWN AND ANTICIPATED COMPLICATIONS TO THESE TYPES OF PROCEDURES AND ARE NOTED IN THE LABELING. THEREFORE, IT WAS DETERMINED THAT THE REPORTED EVENT WAS AN ANTICIPATED PATIENT COMPLICATION.

Additional Manufacturer Narrative · 1

PMA/510(K)# - K031049 / K042539. COMPLAINT SOURCE ¿ LITERATURE: YONG SAM SHIN ET AL. J KOREAN NEUROSURGICAL SOCIETY 54 : 19-24, 2013. THE DEVICE REMAINS IMPLANTED.

Description of Event or Problem · 1

IT WAS REPORTED IN AN ARTICLE IN KOREAN NEUROSURGICAL SOCIETY THAT POST COIL EMBOLIZATION OF THE UNRUPTURED POSTERIOR INFERIOR CEREBELLAR ARTERY (PICA) ANEURYSM, THE PATIENT SUFFERED HEADACHE AND DIZZINESS. SEVERAL DIFFUSION-WEIGHTED IMAGING POSITIVE LESIONS (DWILS) WERE DETECTED IN IPSILATERAL PICA TERRITORY INDICATIVE OF A THROMBOEMBOLIC EVENT. THE SYMPTOMS IMPROVED COMPLETELY AT DISCHARGE. THE PATIENT UNDERWENT THE PROCEDURE BETWEEN JANUARY 2010 AND MARCH 2012. THE EXACT DATE OF THE PROCEDURE IS UNKNOWN.

Description of Event or Problem · 1

IT WAS REPORTED IN AN ARTICLE IN KOREAN NEUROSURGICAL SOCIETY THAT POST COIL EMBOLIZATION OF THE UNRUPTURED POSTERIOR INFERIOR CEREBELLAR ARTERY (PICA) ANEURYSM, THE PATIENT SUFFERED HEADACHE AND DIZZINESS. SEVERAL DIFFUSION-WEIGHTED IMAGING POSITIVE LESIONS (DWILS) WERE DETECTED IN IPSILATERAL PICA TERRITORY INDICATIVE OF A THROMBOEMBOLIC EVENT. THE SYMPTOMS IMPROVED COMPLETELY AT DISCHARGE. THE PATIENT UNDERWENT THE PROCEDURE BETWEEN (B)(6) 2010 AND (B)(6) 2012. THE EXACT DATE OF THE PROCEDURE IS UNKNOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
489601 UNKNOWN_NEUROVASCULAR_PRODUCT DEVICE, NEUROVASCULAR EMBOLIZATION HCG STRYKER NEUROVASCULAR CORK

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other TWO GDC COILS (STRYKER)