Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:14365
Brand Name:Hospira GemStar Infusion pump
Model:All models
Affected:All serial numbers
Software version:
Recalling Organisation:Hospira NZ Ltd
58 Richard Pearse Drive
Airport Oaks
Mangere
Auckland 2022
Contact Information:04 384 7463
Manufacturer:Hospira Inc
Issue:The proximal and distal pressure sensor calibration can drift resulting in the pump failing the Proximal or Distal Occlusion Operational Test, as described in the GemStar Technical Service Manual (TSM). A pump with this issue may, instead of reporting an error, not detect occlusions or issue false occlusion alarms, which will stop the infusion and invoke visual and audible warnings to the user.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:3/4/2013
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