FDA Adverse Event Summary report: N

SPECTRUM TURBO-JECT MINOCYCLINE

MDR report key: 1913261 · Received November 17, 2010

Report

Report Number
1913261
Date Received
November 17, 2010
Date of Event
November 5, 2010
Report Date
November 17, 2010
Manufacturer
COOK MEDICAL INC.
Product Code
LJS
Report Source
User Facility report
Reporter Location
UT, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

PICC TEAM WAS PLACING A PICC LINE. DURING THE PROCEDURE THE GUIDE WIRE BEGAN TO FRAY. IT WAS DIFFICULT TO PULL OUT OF THE PATIENT'S TISSUE. ONCE PULLED OUT, IT WAS CHECKED TO MAKE SURE IT WAS INTACT. THE WIRE AND THE NEEDLE WERE PLACED IN A HAZARDOUS WASTE CONTAINER TO BE GIVEN TO THE REP OF THE MANUFACTURER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPECTRUM TURBO-JECT MINOCYCLINE CATHETER, PICC LJS COOK MEDICAL INC. * *

Patients

Seq Age Sex Outcome Treatment
1 77 YR