{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Mounds View",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93401",
      "recalling_firm": "Medtronic Inc.",
      "address_1": "8200 Coral Sea St Ne",
      "address_2": "N/A",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Foreign Distribution",
      "recall_number": "Z-0522-2024",
      "product_description": "Medtronic SynchroMed, Model A10",
      "product_quantity": "2543 units",
      "reason_for_recall": "The previous software application version (1.1.300) is missing a decimal separator (a comma) for parameter range guidance values displayed on some of the programming screens:  Catheter, Reservoir, Infusion, Bolus, myPTM, and Alarm.",
      "recall_initiation_date": "20200713",
      "center_classification_date": "20231209",
      "report_date": "20231220",
      "code_info": "GTIN 00643169771031, All serial numbers with software version 1.1.300."
    }
  ]
}