Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:16406
Brand Name:Maquet Intra-Aortic Balloon Pump
Model:Models: System 98, System 98XT, CS100, CS100i and CS300
Affected:
Software version:
Recalling Organisation:Maquet Australia Pty Ltd (NZ)
12G Andromeda Cres East Tamaki
Auckland 2013
Contact Information:021 874 882
Manufacturer:Datascope Corporation
Issue:The manufacturer has issued a notice to emphasize the importance of battery maintenance of MAQUET's Intra-aortic balloon pumps (IABP) in accordance with MAQUET's Operating Instructions & Service Manuals.
Recall action type:Alert
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:2/4/2014
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