FDA Adverse Event Malfunction Summary report: N

JET CIRCUIT

MDR report key: 556352 · Received August 25, 2004

Report

Report Number
MW1033056
Event Type
Malfunction
Date Received
August 25, 2004
Date of Event
August 23, 2004
Report Date
August 24, 2004
Manufacturer
BUNNELL INC.
Product Code
BZO
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

TUBING WAS DETACHED FROM PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 JET CIRCUIT JET CIRCUIT BZO BUNNELL INC. * 4D0148

Patients

Seq Age Sex Outcome Treatment
1 * Other