{
  "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": "2026-08-19",
    "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": "96237",
      "recalling_firm": "Medtronic Neuromodulation",
      "address_1": "7000 Central Ave Ne",
      "address_2": "",
      "postal_code": "55432-3568",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Canary Islands, Czech Republic, France, Germany, Greece, Ireland, Italy, Netherlands, Norway, Portugal, Puerto Rico, Spain, Sweden, Switzerland, United Kingdom.",
      "recall_number": "Z-1506-2025",
      "product_description": "A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.",
      "product_quantity": "4365 units",
      "reason_for_recall": "Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.",
      "recall_initiation_date": "20250109",
      "center_classification_date": "20250401",
      "report_date": "20250409",
      "code_info": "version v.2x, UDI/DI 00763000632793",
      "more_code_info": ""
    }
  ]
}