Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18902
Brand Name:Medtronic Activa PC 37601 Neurostimulator
Model:37601
Affected:All serial numbers
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Brand Name:Medtronic Activa SC Model 37603 Neurostimulator
Model:37603
Affected:All serial numbers
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Brand Name:Medtronic ACTIVA RC 37612 Neurostimulator
Model:37612
Affected:All serial numbers
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Brand Name:Medtronic Model 7428 Kinetra Neurostimulator
Model:7428
Affected:All serial numbers
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Brand Name:Medtronic Model 7426 Soletra Neurostimulator
Model:7426
Affected:All serial numbers
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Brand Name:Medtronic Activa SC Model 37602 Neurostimulator
Model:37602
Affected:All serial numbers
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Issue:Following monitoring of reported events, clinical trials and published literature, Medtronic has updated the Warnings and Adverse Events sections. The labelling updates potential risks which have been reported with Deep Brain Stimulation therapy.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Healthcare Professional
Date Commenced:30/7/2015
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