FDA Adverse Event Malfunction Summary report: N

HSR-4000

MDR report key: 177711 · Received June 29, 1998

Report

Report Number
6000002-1998-00152
Event Type
Malfunction
Date Received
June 29, 1998
Date of Event
May 29, 1998
Report Date
June 1, 1998
Manufacturer
BAXTER HEALTHCARE CORP
Product Code
DTN
Product Problem
Yes
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HSR-4000 VENOUS RESERVOIR DTN BAXTER HEALTHCARE CORP HSR-4000 PP7D2836

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN