Reported Jan 18, 2023 · Ongoing
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900B
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 CT900B
- Lot codes and dates
- GTIN 00643169890947Serial/Lot
- Numbers
362 of 362 codes
NPL1001759NPL1002443NPL1000118NPL1001372NPL1001373NPL1000135NPL1000138NPL1000062NPL1000060NPL1001408NPL1001241NPL1002741NPL1002730NPL1000183NPL1001773NPL1001678NPL1000332NPL1000065NPL1000073NPL1000281NPL1000301NPL1001551NPL1001687NPL1001711NPL1001712NPL1001717NPL1001724NPL1001728NPL1001740NPL1001754NPL1001769NPL1001793NPL1001812NPL1001813NPL1001816NPL1001823NPL1001885NPL1001887NPL1001995NPL1001996NPL1002426NPL1000067NPL1000069NPL1000074NPL1000296NPL1000303NPL1000361NPL1000362NPL1000483NPL1000485NPL1000486NPL1000487NPL1001520NPL1001549NPL1001705NPL1001716NPL1001723NPL1001727NPL1001746NPL1001748
- Amount recalled
- 362 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.
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