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

    • NPL1001759
    • NPL1002443
    • NPL1000118
    • NPL1001372
    • NPL1001373
    • NPL1000135
    • NPL1000138
    • NPL1000062
    • NPL1000060
    • NPL1001408
    • NPL1001241
    • NPL1002741
    • NPL1002730
    • NPL1000183
    • NPL1001773
    • NPL1001678
    • NPL1000332
    • NPL1000065
    • NPL1000073
    • NPL1000281
    • NPL1000301
    • NPL1001551
    • NPL1001687
    • NPL1001711
    • NPL1001712
    • NPL1001717
    • NPL1001724
    • NPL1001728
    • NPL1001740
    • NPL1001754
    • NPL1001769
    • NPL1001793
    • NPL1001812
    • NPL1001813
    • NPL1001816
    • NPL1001823
    • NPL1001885
    • NPL1001887
    • NPL1001995
    • NPL1001996
    • NPL1002426
    • NPL1000067
    • NPL1000069
    • NPL1000074
    • NPL1000296
    • NPL1000303
    • NPL1000361
    • NPL1000362
    • NPL1000483
    • NPL1000485
    • NPL1000486
    • NPL1000487
    • NPL1001520
    • NPL1001549
    • NPL1001705
    • NPL1001716
    • NPL1001723
    • NPL1001727
    • NPL1001746
    • NPL1001748
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.

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.

Free recall alerts

Get alerted about new Medtronic Neuromodulation recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:45 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.