FDA Adverse Event Malfunction Summary report: N

6000030-2006-00073

MDR report key: 666848 · Received January 13, 2006

Report

Report Number
6000030-2006-00073
Event Type
Malfunction
Date Received
January 13, 2006
Date of Event
December 12, 2005
Report Date
January 6, 2006
Manufacturer
RICE CREEK MFG
Product Code
LKK
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LKK RICE CREEK MFG 862718 NA

Patients

Seq Age Sex Outcome Treatment
1 35 YR