FDA Device recall Z-0914-2023
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D
- FDA Device
- Class II
- ongoing
- Published 2023-01-18
On 2023-01-18 the FDA classified a Class II recall of Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D by Medtronic Neuromodulation, citing software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303".
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0914-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-12-03 |
| Published | 2023-01-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Neuromodulation |
| Distribution | n/a |
Product
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D
Reason
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
Identifiers
| code_info | GTIN 00763000077730: Serial/Lot Numbers: NPL3007591, NPL3013601, NPL3001811, NPL3006844, NPL3002246, NPL3011056, NPL3…GTIN 00763000077730: Serial/Lot Numbers: NPL3007591, NPL3013601, NPL3001811, NPL3006844, NPL3002246, NPL3011056, NPL3014275, NPL3000542, NPL3015356, NPL3006821, NPL3006824, NPL3013679, NPL3008056, NPL3015357, NPL3015563, NPL3014832, NPL3014949, NPL3015345, NPL3001926, NPL3015319, NPL3015415, NPL3013655, NPL3014617, NPL3014694, NPL3014695, NPL3015349, NPL3015556, NPL3005199, NPL3007777, NPL3007423, NPL3014418, NPL3011745, NPL3001266, NPL3011265, NPL3014842, NPL3010928, NPL3014927, NPL3014877, NPL3014706, NPL3010720, NPL3004487, NPL3014750, NPL3006084, NPL3010654, NPL3015557, NPL3013639, NPL3015561, NPL3004626, NPL3014605, NPL3014916, NPL3000681, NPL3014315, NPL3007571, NPL3013786, NPL3011225, NPL3004327, NPL3014738, NPL3015555, NPL3013646, NPL3000396, NPL3014857, NPL3014859, NPL3015545, NPL3015546, NPL3015547, NPL3015548, NPL3011797, NPL3011799, NPL3014698, NPL3003566, NPL3011541, NPL3015537, NPL3015538, NPL3002352, NPL3004707, NPL3014215, NPL3015527, NPL3005214, NPL3013913, NPL301533 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0914-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.