CanadaThe Vanta/Sequentia Lt Clinician Programmer Application (Medtronic model A71200, app versions V2.0.2465 and V2.0.2683) is affected; it may display a “system error” if the user presses the start usage button twice when interrogating a new implantable neurostimulator and then show a subsequent “validation error” that can prevent completing the first interrogation. Contact the manufacturer, Medtronic Inc., for additional information.
What's being recalled
Companies: Medtronic Inc., 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432.
How to identify it
Affected products: Vanta/Sequentia Lt Clinician Programmer Application; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: A71200
The hazard
The Vanta A71200 CP app V2.0.2465 and V2.0.2683 will display a "system error" if the user selects the start usage button twice when interrogating a new implantable neurostimulator (INS). This error prompts the user to restart the CP app and contact Medtronic for assistance. Upon subsequent interrogation of the INS, the Vanta A71200 CP app will display a "validation error" prompting the user to resolve the error in order to proceed with the INS interrogation. If the validation error is not resolved, the user is unable to complete the first attempt at interrogating the INS.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)