FDA Adverse Event Summary report: N

INFUSOMAT SPACE - US VERSION

MDR report key: 3769867 · Received April 17, 2014

Report

Report Number
2523676-2014-00123
Date Received
April 17, 2014
Date of Event
August 26, 2013
Report Date
March 21, 2014
Manufacturer
B. BRAUN MELSUNGEN AG
Product Code
FRN
Product Problem
Yes
Report Source
Distributor report
Reporter Location
MO, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

AS REPORTED BY THE USER FACILITY: TRANSFUSING BLOOD PUMP JNE 4130 REPEATEDLY ALARMING AIR. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
236671 INFUSOMAT SPACE - US VERSION INFUSION PUMP FRN B. BRAUN MELSUNGEN AG NA NA

Patients

Seq Age Sex Outcome Treatment
1 UNK