Medtronic recalls Vanta/Seqenita LT Clinician Programmer (Model CT900D) due to software anomalies causing messages like 'Too Many Device Found' and 'Unexpected Device Error Code 1502'.
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
Medtronic is recalling Vanta/Seqenita LT Clinician Programmer applications (Model CT900D) because they display software errors that could cause device issues. This affects specific units with serial numbers listed in the recall.
The software anomalies cause the device to display error messages such as 'Too Many Device Found', 'Unexpected Device Error Code 1502', and 'System Update Needed, Service Code 303'. These messages indicate potential issues that could affect device functionality but do not pose a direct risk of injury.
Users of Medtronic Vanta/Seqenita LT Clinician Programmer applications (Model CT900D) with the listed serial numbers are affected. Patients using these devices for pain therapy may be at risk if they encounter software errors.
Check if your Vanta/Seqenita LT Clinician Programmer (Model CT900D) has a serial number listed in the provided list of serial numbers (NPL3007591, NPL3013601, etc.) or GTIN numbers (00763000077730, 00763000094027, 00763000421007).
Review your device for error messages like 'Too Many Device Found' or 'Unexpected Device Error Code 1502'.
Reach out to Medtronic for guidance on resolving software issues or updating the device.
The model number is CT900D for Vanta/Seqenita LT Clinician Programmer applications.
Check if your serial number is listed in the provided list of serial numbers (NPL3007591, NPL3013601, etc.) or GTIN numbers (00763000077730, 00763000094027, 00763000421007).
No, the recall does not require immediate discontinuation. The software errors are not a direct risk of injury but may affect device functionality.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0914-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0914-2023 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
