Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18142
Brand Name:GE Patient Monitor, Multiparameter
Model:Models: B20 V1, B30, B40 V1, B40 V2
Affected:
Software version:
Recalling Organisation:GE Healthcare Limited
Level 7, Vero Centre
48 Shortland St
Auckland 1010
Contact Information:0800 659 465
Manufacturer:GE Medical Systems Information Technologies Inc
Brand Name:GE Carescape B850 Patient Monitor, Multi-Parameter
Model:B850
Affected:
Software version:
Recalling Organisation:GE Healthcare Limited
Level 7, Vero Centre
48 Shortland St
Auckland 1010
Contact Information:0800 659 465
Manufacturer:GE Healthcare Finland Oy
Issue:GE Healthcare has recently become aware of potential inconsistencies in the completion of certain device corrections related to the subject product corrections. Devices are to be inspected to ensure the previous corrective actions have been conducted appropriately.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:24/2/2015
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