FDA Adverse Event Injury Summary report: N

HUMMINGBIRD VENTRICULAR

MDR report key: 5048851 · Received August 12, 2015

Report

Report Number
5048851
Event Type
Injury
Date Received
August 12, 2015
Date of Event
August 1, 2015
Report Date
August 11, 2015
Manufacturer
INNERSPACE INC.
Product Code
HCA
Product Problem
Yes
Report Source
User Facility report
Reporter Location
HI, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

DURING PLACEMENT OF THE VENTRICULOSTOMY CATHETER THE FIRST CATHETER INSERTED UNFORTUNATELY WAS FRACTURED OR LACERATED BY THE INNER TABLE AND A FRAGMENT OF CATHETER WAS LEFT IN SITU.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
532302 HUMMINGBIRD VENTRICULAR VENTRICULAR CATHETER HCA INNERSPACE INC. H200MR 140616-03

Patients

Seq Age Sex Outcome Treatment
1 24 YR Hospitalization