FDA Adverse Event Injury Summary report: N

STENT - VASCULAR RECONSTRUCTION

MDR report key: 7978799 · Received October 18, 2018

Report

Report Number
1226348-2018-00741
Event Type
Injury
Date Received
October 18, 2018
Date of Event
December 31, 2012
Report Date
September 24, 2018
Manufacturer
CODMAN AND SHURTLEFF, INC
Product Code
NJE
PMA / PMN Number
H60001
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). SINCE THE PRODUCT WAS NOT RETURNED FOR ANALYSIS, NO PRODUCT FAILURE ANALYSIS CAN BE CONDUCTED AND NO DETERMINATION OF POSSIBLE CONTRIBUTING FACTORS COULD BE MADE. DEVICE HISTORY RECORD (DHR) REVIEW CANNOT BE CONDUCTED BECAUSE THE NO LOT NUMBER WAS PROVIDED BY THE CUSTOMER.

Description of Event or Problem · 1

THIS COMPLAINT IS FROM A LITERATURE SOURCE. AS REPORTED IN THE LITERATURE PUBLICATION ENTITLED, ¿THE PENUMBRA COIL 400 SYSTEM FOR TREATMENT OF WIDE-NECKED INTRACRANIAL ANEURYSMS: INITIAL SINGLE-CENTER EXPERIENCE¿: A PATIENT FROM A GROUP ¿PENUMBRA COIL 400 SYSTEM¿ WITH WIDE-NECKED INTRACRANIAL ANEURYSM UNDERWENT THE ENTERPRISE STENT-ASSISTED COIL (SAC) EMBOLIZATION, SUFFERED AN ANEURYSM WORSENED FROM COMPLETE OBLITERATION TO A SMALL RESIDUAL NECK WITH RECOMMENDED OBSERVATION RATHER THAN TREATMENT. TITLE: ¿ THE PENUMBRA COIL 400 SYSTEM FOR TREATMENT OF WIDE-NECKED INTRACRANIAL ANEURYSMS: INITIAL SINGLE-CENTER EXPERIENCE. ¿ THE PURPOSE OF THIS STUDY WAS TO EXAMINE THE FREQUENCY OF ADJUNCTIVE STENT USAGE WHEN COILING WIDE-NECKED INTRACRANIAL ANEURYSMS WITH THE PC-400 IN COMPARISON WITH CONVENTIONAL COILS. METHOD: BETWEEN OCTOBER 2008 AND DECEMBER 2012. PATIENTS WERE DIVIDED INTO TWO GROUPS BASED ON THE CHOICE OF ENDOVASCULAR COILS: PC-400 AND CONVENTIONAL COILS (CASHMERE, MICRUSPHERE, DELTAWIND, AND ULTIPAQ: CODMAN & SHURTLEFF, INC., RAYNHAM MA, USA; HYDROGEL, COSMOS, COMPLEX, AND HYPERSOFT: MICROVENTION, INC., TUSTIN CA, USA). ALL PATIENTS HAD PLANNED ADJUNCTIVE STENTING WITH EITHER AN ENTERPRISE (CODMAN & SHURTLEFF, INC., RAYNHAM MA, USA) OR NEUROFORM (STRYKER CORPORATION, KALAMAZOO MI, USA) INTRACRANIAL STENT. ONLY UNRUPTURED ANEURYSMS WERE CONSIDERED IN THE PRESENT ANALYSIS BECAUSE ADJUNCTIVE STENT PLACEMENT IS A RARITY AFTER ANEURYSM SUBARACHNOID HEMORRHAGE WHERE ANTIPLATELET THERAPY IS A RELATIVE CONTRAINDICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
818205 STENT - VASCULAR RECONSTRUCTION INTRACRANIAL NEUROVASCULAR STENT NJE CODMAN AND SHURTLEFF, INC

Patients

Seq Age Sex Outcome Treatment
1 59 YR Other