Data Foundry

Medical device recalls 2023

Vanta/Seqenita LT Clinician Programmer Application — Class II medical device recall Z-0914-2023

Ongoing recall by Medtronic Neuromodulation, reported 2023-01-18. Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System

Recall numberZ-0914-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedtronic Neuromodulation, Minneapolis, MN, United States
Recall initiated2022-12-03
Classified2023-01-06
Reported by FDA2023-01-18
Quantity1,337 units
Reason classessoftware
UPC / GTIN / UDI-DI00763000077730, 00763000094027, 00763000421007
Lot numbersNPL3000010, NPL3000014, NPL3000017, NPL3000024, NPL3000026, NPL3000029, NPL3000031, NPL3000035, NPL3000042, NPL3000043, NPL3000047, NPL3000050, NPL3000056, NPL3000057, NPL3000058, NPL3000060, NPL3000066, NPL3000083, NPL3000098, NPL3000107, NPL3000120, NPL3000125, NPL3000135, NPL3000141, NPL3000143, NPL3000184, NPL3000187, NPL3000191, NPL3000192, NPL3000203, NPL3000208, NPL3000209, NPL3000212, NPL3000215, NPL3000223, NPL3000241, NPL3000244, NPL3000248, NPL3000249, NPL3000250 and 460 more
Model numbersCT900D

Product

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"

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0914-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.