FDA Adverse Event Malfunction Summary report: N

ENROUTE TRANSCAROTID NEUROPROTECTION SYSTEM

MDR report key: 18169331 · Received November 20, 2023

Report

Report Number
18169331
Event Type
Malfunction
Date Received
November 20, 2023
Date of Event
June 30, 2023
Report Date
July 24, 2023
Manufacturer
SILK ROAD MEDICAL, INC.
Product Code
NTE
UDI-DI
00811311020829
Product Problem
Yes
Report Source
User Facility report
Reporter Location
VA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

VALVE ON VENOUS SHEATH VERY DIFFICULT TO PASS DILATOR THROUGH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1688224 ENROUTE TRANSCAROTID NEUROPROTECTION SYSTEM TEMPORARY CAROTID CATHETER FOR EMBOLIC CAPTURE NTE SILK ROAD MEDICAL, INC. FG12522 303160 00811311020829

Patients

Seq Age Sex Outcome Treatment
1 21900 DA Male