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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:197401

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C

Official recall number

Z-0913-2023

Evidence summary

Product code
LGW
Recall status
Open, Classified
Event initiated
December 03, 2022
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0913-2023