PlainRecalls
FDA Devices Moderate Class II Ongoing

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D

Reported: January 18, 2023 Initiated: December 3, 2022 #Z-0914-2023

Product Description

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D

Reason for Recall

Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"

Details

Recalling Firm
Medtronic Neuromodulation
Units Affected
1337 units
Distribution
Worldwide distribution.
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D. Recalled by Medtronic Neuromodulation. Units affected: 1337 units.
Why was this product recalled?
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
Which agency issued this recall?
This recall was issued by the FDA Devices on January 18, 2023. Severity: Moderate. Recall number: Z-0914-2023.