Reported Jan 18, 2023 · Ongoing

Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900D

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 CT900D
Lot codes and dates
  • GTIN 00763000077730Serial/Lot
  • Numbers

    824 of 824 codes

    • NPL3007591
    • NPL3013601
    • NPL3001811
    • NPL3006844
    • NPL3002246
    • NPL3011056
    • NPL3014275
    • NPL3000542
    • NPL3015356
    • NPL3006821
    • NPL3006824
    • NPL3013679
    • NPL3008056
    • NPL3015357
    • NPL3015563
    • NPL3014832
    • NPL3014949
    • NPL3015345
    • NPL3001926
    • NPL3015319
    • NPL3015415
    • NPL3013655
    • NPL3014617
    • NPL3014694
    • NPL3014695
    • NPL3015349
    • NPL3015556
    • NPL3005199
    • NPL3007777
    • NPL3007423
    • NPL3014418
    • NPL3011745
    • NPL3001266
    • NPL3011265
    • NPL3014842
    • NPL3010928
    • NPL3014927
    • NPL3014877
    • NPL3014706
    • NPL3010720
    • NPL3004487
    • NPL3014750
    • NPL3006084
    • NPL3010654
    • NPL3015557
    • NPL3013639
    • NPL3015561
    • NPL3004626
    • NPL3014605
    • NPL3014916
    • NPL3000681
    • NPL3014315
    • NPL3007571
    • NPL3013786
    • NPL3011225
    • NPL3004327
    • NPL3014738
    • NPL3015555
    • NPL3013646
    • NPL3000396
  • GTIN 00763000094027Serial/Lot
  • Numbers

    127 of 127 codes

    • NPL3019673
    • NPL3019538
    • NPL3019537
    • NPL3019769
    • NPL3019539
    • NPL3017933
    • NPL3018885
    • NPL3018890
    • NPL3018889
    • NPL3018718
    • NPL3018888
    • NPL3018719
    • NPL3018715
    • NPL3018716
    • NPL3018577
    • NPL3017991
    • NPL3017992
    • NPL3017993
    • NPL3017915
    • NPL3017269
    • NPL3017270
    • NPL3017266
    • NPL3017265
    • NPL3017268
    • NPL3017262
    • NPL3017261
    • NPL3017286
    • NPL3017249
    • NPL3017248
    • NPL3017277
    • NPL3017281
    • NPL3017280
    • NPL3017254
    • NPL3017255
    • NPL3014530
    • NPL3014346
    • NPL3003700
    • NPL3014098
    • NPL3014500
    • NPL3014079
    • NPL3014066
    • NPL3014045
    • NPL3014043
    • NPL3014040
    • NPL3013708
    • NPL3011300
    • NPL3011350
    • NPL3011362
    • NPL3011363
    • NPL3010736
    • NPL3010759
    • NPL3007387
    • NPL3003716
    • NPL3000187
    • NPL3000191
    • NPL3000192
    • NPL3002273
    • NPL3002278
    • NPL3002283
    • NPL3002306
  • GTIN 00763000421007Serial/Lot
  • Numbers

    386 of 386 codes

    • NPL3021063
    • NPL3021064
    • NPL3021347
    • NPL3017616
    • NPL3019755
    • NPL3020234
    • NPL3020814
    • NPL3021232
    • NPL3021418
    • NPL3020142
    • NPL3020904
    • NPL3020871
    • NPL3020875
    • NPL3021565
    • NPL3018628
    • NPL3018512
    • NPL3020262
    • NPL3017958
    • NPL3018626
    • NPL3020970
    • NPL3016949
    • NPL3021006
    • NPL3017503
    • NPL3019879
    • NPL3021003
    • NPL3021288
    • NPL3021295
    • NPL3021306
    • NPL3021407
    • NPL3021448
    • NPL3019561
    • NPL3017149
    • NPL3017535
    • NPL3020026
    • NPL3020774
    • NPL3020775
    • NPL3020792
    • NPL3021247
    • NPL3020159
    • NPL3020160
    • NPL3017413
    • NPL3020931
    • NPL3018507
    • NPL3018508
    • NPL3019685
    • NPL3020738
    • NPL3020740
    • NPL3017110
    • NPL3020766
    • NPL3020767
    • NPL3021196
    • NPL3020888
    • NPL3020905
    • NPL3020002
    • NPL3020005
    • NPL3019630
    • NPL3017530
    • NPL3020170
    • NPL3018544
    • NPL3019703
Amount recalled
1337 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, 5:45 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.