FDA Adverse Event Injury Summary report: N

HORIZON MEDICAL PRODUCTS, INC.

MDR report key: 300360 · Received October 11, 2000

Report

Report Number
MW1020156
Event Type
Injury
Date Received
October 11, 2000
Date of Event
October 3, 2000
Report Date
October 11, 2000
Manufacturer
HORIZON MED. PRODUCTS, INC.
Product Code
LJT
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
NJ, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PORT-A-CATH BROKE AND LODGED ITSELF IN PT'S HEART.

Description of Event or Problem · 1

ADD'L INFO REC'D 10/23/00: AGE OF DEVICE: 6 MOS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HORIZON MEDICAL PRODUCTS, INC. LIFE PORT LJT HORIZON MED. PRODUCTS, INC. 7013 14899

Patients

Seq Age Sex Outcome Treatment
1 69 YR Life Threatening