Reported Jan 18, 2023 · Ongoing
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900E
Medtronic Neuromodulation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Neuromodulation · 7000 Central Ave Ne · Minneapolis, MN · 55432-3568
Is this the product you have?
- Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900E
- Lot codes and dates
- GTIN 00763000447090Serial/Lot
- Numbers
NPL3022869NPL3022873NPL3022049NPL3022050NPL3022795NPL3022817NPL3022190NPL3022191NPL3022052NPL3022187NPL3022193NPL3022194NPL3022195NPL3022212NPL3022213NPL3022289NPL3021964NPL3022043NPL3022044NPL3022034NPL3021984NPL3021990
- Amount recalled
- 22 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Why it was recalled
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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