Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:14791
Brand Name:CareFusion Alaris GP, GP Guardrails, GP Plus & GP Plus Guardrails Infusion Pumps
Model:Models: 80263UN01, 80263UN01-G, 9002MED01, 9002MED01-G
Affected:Pumps manufactured between Dec 2009 and Jan 2012
Software version:
Recalling Organisation:CareFusion New Zealand 313 Limited
Unit 4 / 110 Mays Road
Onehunga
AUCKLAND 1061
Contact Information:0508 422 734
Manufacturer:CareFusion Switzerland 317 Sarl
Issue:The manufacturer has identified an increased occurrence of stepper motor stalls with selected models of Alaris GP infusion pump. It has been determined that these stalls are due to the stepper motor's front and rear bearings which may not perform as designed after a period of use causing the pump to stop infusing.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:11/6/2013
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