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
NPL3007591NPL3013601NPL3001811NPL3006844NPL3002246NPL3011056NPL3014275NPL3000542NPL3015356NPL3006821NPL3006824NPL3013679NPL3008056NPL3015357NPL3015563NPL3014832NPL3014949NPL3015345NPL3001926NPL3015319NPL3015415NPL3013655NPL3014617NPL3014694NPL3014695NPL3015349NPL3015556NPL3005199NPL3007777NPL3007423NPL3014418NPL3011745NPL3001266NPL3011265NPL3014842NPL3010928NPL3014927NPL3014877NPL3014706NPL3010720NPL3004487NPL3014750NPL3006084NPL3010654NPL3015557NPL3013639NPL3015561NPL3004626NPL3014605NPL3014916NPL3000681NPL3014315NPL3007571NPL3013786NPL3011225NPL3004327NPL3014738NPL3015555NPL3013646NPL3000396
- GTIN 00763000094027Serial/Lot
- Numbers
127 of 127 codes
NPL3019673NPL3019538NPL3019537NPL3019769NPL3019539NPL3017933NPL3018885NPL3018890NPL3018889NPL3018718NPL3018888NPL3018719NPL3018715NPL3018716NPL3018577NPL3017991NPL3017992NPL3017993NPL3017915NPL3017269NPL3017270NPL3017266NPL3017265NPL3017268NPL3017262NPL3017261NPL3017286NPL3017249NPL3017248NPL3017277NPL3017281NPL3017280NPL3017254NPL3017255NPL3014530NPL3014346NPL3003700NPL3014098NPL3014500NPL3014079NPL3014066NPL3014045NPL3014043NPL3014040NPL3013708NPL3011300NPL3011350NPL3011362NPL3011363NPL3010736NPL3010759NPL3007387NPL3003716NPL3000187NPL3000191NPL3000192NPL3002273NPL3002278NPL3002283NPL3002306
- GTIN 00763000421007Serial/Lot
- Numbers
386 of 386 codes
NPL3021063NPL3021064NPL3021347NPL3017616NPL3019755NPL3020234NPL3020814NPL3021232NPL3021418NPL3020142NPL3020904NPL3020871NPL3020875NPL3021565NPL3018628NPL3018512NPL3020262NPL3017958NPL3018626NPL3020970NPL3016949NPL3021006NPL3017503NPL3019879NPL3021003NPL3021288NPL3021295NPL3021306NPL3021407NPL3021448NPL3019561NPL3017149NPL3017535NPL3020026NPL3020774NPL3020775NPL3020792NPL3021247NPL3020159NPL3020160NPL3017413NPL3020931NPL3018507NPL3018508NPL3019685NPL3020738NPL3020740NPL3017110NPL3020766NPL3020767NPL3021196NPL3020888NPL3020905NPL3020002NPL3020005NPL3019630NPL3017530NPL3020170NPL3018544NPL3019703
- 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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