Product Wiki · Recalls · Health Canada — Medical Devices

CT900 Clinician Programmer Software Application A710 Intellis & A810… — recall 59899

Health Canada — Medical Devices · Canada · 2019-08-23 · Type III

As described by Health Canada — Medical Devices: CT900 Clinician Programmer Software Application A710 Intellis & A810 Synchromed (2019-07-29)

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Agency
Health Canada — Medical Devices
Recall identifier
59899
Date of alert
2019-08-23
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Medtronic is informing customers that records do not match the country registration associated with the CT900 Clinician Tablet(s) associated with customer accounts. If the wrong country is selected during CT900 tablet registration, the following may occur: Customers may have access to applications that are not approved in their country. Customers may not have access to applications that are approved in their country.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ct900-clinician-programmer-sof

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