Medtronic recalls Vanta/Seqenita LT Clinician Programmer Application (Model CT900B) due to software anomalies causing error 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 CT900B) that may display software error messages. These messages could indicate issues with the device that might affect pain therapy systems.
The software anomalies cause 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 with the device that could affect its proper functioning in pain therapy systems.
Users of Medtronic's Vanta/Seqenita LT Clinician Programmer Application (Model CT900B) for pain therapy systems. Patients using these devices for pain management are most at risk.
Check for the model number CT900B on the device. The serial numbers listed in the recall include NPL1001759 and other numbers starting with NPL1000000. The product was sold with GTIN 00643169890947.
Look for error messages like 'Too Many Device Found', 'Unexpected Device Error Code 1502', or 'System Update Needed, Service Code 303' on the device screen.
The model number is CT900B for the Vanta/Seqenita LT Clinician Programmer Application.
The device may display 'Too Many Device Found', 'Unexpected Device Error Code 1502', or 'System Update Needed, Service Code 303'.
Check the serial number on your device. The recall includes serial numbers starting with NPL1000000, such as NPL1001759.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0912-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0912-2023 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.
