FDA Adverse Event Malfunction Summary report: N

HAMILTON MEDICAL, INC.

MDR report key: 350554 · Received September 6, 2001

Report

Report Number
2937708-2001-00004
Event Type
Malfunction
Date Received
September 6, 2001
Manufacturer
HAMILTON MEDICAL, INC.
Product Code
BYE
Report Source
Manufacturer report
Reporter Location
NV, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

BIOMEDICAL ENGINEER AT HOSPITAL WAS INTERVIEWED IN 2001. PER THE INTERVIEW, ALADDIN II HAD THE DISPLAY BLINKING ON AND OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
40647 HAMILTON MEDICAL, INC. NASAL CPAP BYE HAMILTON MEDICAL, INC. ALADDINII *

Patients

Seq Age Sex Outcome Treatment
1 *