FDA Adverse Event Other Summary report: N

9611112-2006-00002

MDR report key: 967183 · Received June 22, 2007

Report

Report Number
9611112-2006-00002
Event Type
Other
Date Received
June 22, 2007
Product Code
FZS
Report Source
Manufacturer report

Narratives

Additional Manufacturer Narrative · 1

THE MFR HAS BEEN NOTIFIED OF THE REPORTED INFO. AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFO.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FZS

Patients

Seq Age Sex Outcome Treatment
1