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Medtronic Neuromodulation Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D - safety alert
Official notice
18 Jan 2023
Last checked
18 Jan 2023
An official FDA notice concerns Medtronic Neuromodulation Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D - safety alert. An official FDA notice concerns Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-01-18. Lots: NPL3007591, NPL3019673, NPL3021063. Recall numbers: Z-0914-2023. Check the official notice for the complete list. Published 2023-01-18.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
1,337
Recall number
Z-0914-2023
Official notice
2023-01-18
The hazard
The hazard
An official FDA notice concerns Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-01-18. Lots: NPL3007591, NPL3019673, NPL3021063. Recall numbers: Z-0914-2023. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
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Company & contacts
Company & contacts
Brand: Medtronic Neuromodulation. Contact: Medtronic Neuromodulation.
Source & status
Source & status
Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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