FDA Adverse Event Malfunction Summary report: N

HIR-200

MDR report key: 430778 · Received November 26, 2002

Report

Report Number
1221261-2002-00086
Event Type
Malfunction
Date Received
November 26, 2002
Report Date
November 15, 2002
Manufacturer
LEVEL 1, INC.
Product Code
KZD
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

HOSPITAL ALLEGES THAT THE FRONT DOOR CAME FLYING OFF OF HIR-200 PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HIR-200 * KZD LEVEL 1, INC. HIR-200 NA

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Other