Reported Jan 18, 2023 · Ongoing

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900A

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 CT900A
Lot codes and dates
  • GTIN 00643169890923Serial/Lot
  • Numbers

    440 of 440 codes

    • NPL0000474
    • NPL0000027
    • NPL0000072
    • NPL0000284
    • NPL0000561
    • NPL0003519
    • NPL0003792
    • NPL0000454
    • NPL0002036
    • NPL0004205
    • NPL0004222
    • NPL0003112
    • NPL0001300
    • NPL0003989
    • NPL0004099
    • NPL0004693
    • NPL0004711
    • NPL0004761
    • NPL0003189
    • NPL0001861
    • NPL0000740
    • NPL0001082
    • NPL0001698
    • NPL0001700
    • NPL0001703
    • NPL0003058
    • NPL0001697
    • NPL0003428
    • NPL0004076
    • NPL0001735
    • NPL0000971
    • NPL0002467
    • NPL0001025
    • NPL0000012
    • NPL0004605
    • NPL0002212
    • NPL0003070
    • NPL0000966
    • NPL0003890
    • NPL0001326
    • NPL0002948
    • NPL0000300
    • NPL0001081
    • NPL0003246
    • NPL0000325
    • NPL0000095
    • NPL0000756
    • NPL0002660
    • NPL0001100
    • NPL0002921
    • NPL0000548
    • NPL0000018
    • NPL0000170
    • NPL0003125
    • NPL0000495
    • NPL0003562
    • NPL0002336
    • NPL0002674
    • NPL0003293
    • NPL0003324
Amount recalled
440 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:22 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.