FDA Adverse Event Malfunction Summary report: N

HSR-4000

MDR report key: 187604 · Received September 15, 1998

Report

Report Number
6000002-1998-00269
Event Type
Malfunction
Date Received
September 15, 1998
Manufacturer
BAXTER HEALTHCARE CORP.
Product Code
DTN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT DURING REWARMING THE VENOUS OUTPORT ADAPTER DROPPED FROM THE HSR-4000 RESERVOIR. NO PT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HSR-4000 VENOUS RESERVOIR DTN BAXTER HEALTHCARE CORP. HSR-4000 PP5D2029

Patients

Seq Age Sex Outcome Treatment
1 * Other