Product Safety Recalls

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Medtronic Neuromodulation Recall 88761

Description: Clinician Programmer Application (CPA) model A610 Clinician Software Application

Medtronic Neuromodulation Recall 88761 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0201-2022
Event ID88761
Event DescriptionClinician Programmer Application (CPA) model A610 Clinician Software Application
Product TypeDevices
DistributionWorldwide distribution - US Nationwide distribution and the countries of Australia, New Zealand, Canada, Europe, India, Japan, Korea, Middle East, Latin America, Africa, SE Asia and China.
Quantity3302
Recall ReasonA software anomaly may occur with the clinician programmer application.
Device Classification20211110
Device Code InfoClinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081
Center Classification Date20211104
Recall Initiation Date20210923
Recalling FirmMedtronic Neuromodulation
Initial Notification Letter
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