{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "217610",
      "product_res_number": "Z-1043-2026",
      "event_date_initiated": "2025-12-03",
      "event_date_posted": "2026-01-09",
      "recall_status": "Open, Classified",
      "res_event_number": "98097",
      "product_code": "LGW",
      "pma_numbers": [
        "P840001S594"
      ],
      "product_description": "A71200 Vanta\" Clinician Programmer Application (CP App) version\n2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).",
      "code_info": "version\n2.0.2465 and 2.0.2683\n\nUDI-DI (GTIN) 00763000520083\n\nAffected product is the software. Implanted Vanta Neurostimulator devices are not affected.",
      "firm_fei_number": "2182207",
      "recalling_firm": "Medtronic Neuromodulation",
      "address_1": "7000 Central Ave Ne",
      "city": "Minneapolis",
      "state": "MN",
      "postal_code": "55432-3568",
      "additional_info_contact": "Naomi Rodiles\n763-514-2000",
      "reason_for_recall": "Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.",
      "root_cause_description": "Software design",
      "action": "On December 3, 2025 the firm distributed Urgent Medical Device Safety Notification letters to affected consignees. Customers were instructed to download and install A81200 CP App v2.0.2684 or any later version.",
      "product_quantity": "7123",
      "distribution_pattern": "Worldwide - US Nationwide distribution.",
      "openfda": {
        "pma_number": [
          "P030017",
          "P130028",
          "P840001",
          "P800040",
          "P010032",
          "P130022",
          "P210037",
          "P190002"
        ],
        "registration_number": [
          "3004209178",
          "2182207",
          "3038429246",
          "3003335547",
          "3005160949",
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          "3019807891",
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          "3006630150",
          "3004519921",
          "2133810",
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        ],
        "fei_number": [
          "3002618605",
          "2182207",
          "3004369318",
          "3005700659",
          "3038429246",
          "3003335547",
          "3005160949",
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          "3003120897",
          "3005210579",
          "3015173212",
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          "3007616088",
          "3019807891",
          "2024311",
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          "1035166",
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          "2182291",
          "3000206435",
          "3013023969",
          "3010086866",
          "3006630150",
          "1928237",
          "2183744",
          "3004593495"
        ],
        "device_name": "Stimulator, Spinal-Cord, Totally Implanted For Pain Relief",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}