FDA Adverse Event Death Summary report: N

1319477-1998-00003

MDR report key: 190337 · Received September 24, 1998

Report

Report Number
1319477-1998-00003
Event Type
Death
Date Received
September 24, 1998
Date of Event
July 14, 1998
Product Code
BZO
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1