{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98028",
      "recalling_firm": "Medtronic Neuromodulation",
      "address_1": "7000 Central Ave Ne",
      "address_2": "N/A",
      "postal_code": "55432-3568",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Argentina, Aruba, Australia,  Austria, Belgium, Bosnia And Herzegovina, Brazil, Canada, Canary Islands, Chile, China,  Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt,  El Salvador, Finland, France, French Polynesia, Germany, Greece, Guatemala, Hong Kong,  Hungary, Iceland, Indonesia, Ireland, Israel, Italy, Japan, Kuwait, Luxembourg, Malaysia,  Malta, Mauritius, Mexico, Namibia, Netherlands, New Zealand, Norway, Oman, Panama,  Peru, Poland, Portugal, Qatar, Reunion, Russia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Uruguay.",
      "recall_number": "Z-0996-2026",
      "product_description": "Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers:    CT900A PROG CT900A CLINICIAN TABLET US  CT900B PROG CT900B CLINICIAN TABLET EU -UK  CT900C PROG CT900C CLINICIAN TABLET UK  CT900D PROG CT900D CLINICIAN TABLET GLOBAL  CT900E PROG CT900E CLINICIAN TABLET GLBL SMSNG  CT900F PROG CT900F CLINICIAN TABLET GLBL SMSNG",
      "product_quantity": "7667 devices",
      "reason_for_recall": "Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of underlying pain symptoms. Resolution would require surgical replacement of the INS.",
      "recall_initiation_date": "20251120",
      "center_classification_date": "20251223",
      "report_date": "20251231",
      "code_info": "CP App: UDI-DI 00763000273668 all software versions prior to v.1.0.4489 are affected  The implanted devices are not affected."
    }
  ]
}