FDA Adverse Event Malfunction Summary report: N

CURLIN 6000

MDR report key: 1892900 · Received November 1, 2010

Report

Report Number
MW5018036
Event Type
Malfunction
Date Received
November 1, 2010
Date of Event
October 24, 2010
Report Date
November 1, 2010
Manufacturer
MOOG
Product Code
FRN
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MN, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

DATE AND TIME NOT SET ALARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CURLIN 6000 CURLIN 6000 FRN MOOG

Patients

Seq Age Sex Outcome Treatment
1 53 YR