Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanta/Seqenita LT Clinician Programmer Application Recalled by Medtronic Neuromodulation Due to Software anomalies, CP App messages: "Too Many Device...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Neuromodulation directly.
Affected Products
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900B
Quantity: 362 units
Why Was This Recalled?
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
Where Was This Sold?
Worldwide distribution.
About Medtronic Neuromodulation
Medtronic Neuromodulation has 95 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report