Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:25177
Brand Name:Therapeutic plasma exchange system
Model:
Affected:Prismaflex System, PRISMAFLEX 4.11, PRISMAFLEX 5.00 ROW, PRISMAFLEX 6.10 ROW, PRISMAFLEX 7.XX ROW
Software version:
Recalling Organisation:Baxter Healthcare Ltd
33 Vestey Drive
Mt Wellington
AUCKLAND
Contact Information:0800 229 837
Manufacturer:Gambro Lundia AB
Issue:The manufacturer will be upgrading the software on Prismaflex control units to reduce the frequency of communication error alarms. All units with software versions 7.20 and below will be upgraded to 7.21 or higher.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:2/10/2019
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