FDA Adverse Event Injury Summary report: N

CUSTOMIZED FLEX-TEND, CUFFLESS

MDR report key: 147974 · Received February 6, 1998

Report

Report Number
1824231-1998-00001
Event Type
Injury
Date Received
February 6, 1998
Date of Event
December 15, 1997
Report Date
January 14, 1998
Manufacturer
BIVONA MEDICAL TECHNOLOGIES
Product Code
BTO
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SW
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

SILICONE "GODS" DESTROYED ON THREE LOCATIONS. THE TUBE HAS BEEN IN PT FOR 2 WEEKS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CUSTOMIZED FLEX-TEND, CUFFLESS TRACHEOSTOMY TUBE BTO BIVONA MEDICAL TECHNOLOGIES C7TTFT604.5006 CL0820

Patients

Seq Age Sex Outcome Treatment
1 7 YR Hospitalization