FDA Adverse Event Malfunction Summary report: N

1418479-2000-00002

MDR report key: 262397 · Received February 11, 2000

Report

Report Number
1418479-2000-00002
Event Type
Malfunction
Date Received
February 11, 2000
Date of Event
November 19, 1999
Product Code
JOP
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1