FDA Adverse Event Malfunction Summary report: N

6000023-1999-00067

MDR report key: 265383 · Received September 8, 1999

Report

Report Number
6000023-1999-00067
Event Type
Malfunction
Date Received
September 8, 1999
Date of Event
June 21, 1999
Removal / Correction Number
NI
Report Source
Manufacturer report
Reporter Occupation
NO INFORMATION

Narratives

Description of Event or Problem · 1

I

Patients

Seq Age Sex Outcome Treatment
1 * Other