{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90106",
      "recalling_firm": "Abbott",
      "address_1": "5050 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-3209",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution to states of: MO, CA, OH, WA and OUS internationally to Italy and Netherlands.",
      "recall_number": "Z-1213-2022",
      "product_description": "FIRMap\" Catheter, 60mm Basket",
      "product_quantity": "40 units",
      "reason_for_recall": "Incorrect product labeling.",
      "recall_initiation_date": "20220428",
      "center_classification_date": "20220601",
      "termination_date": "20240618",
      "report_date": "20220608",
      "code_info": "Model Number: AR064060; UDI Number: ( 01) 0 0810591 02002 4 ( 17) 020531 ( 00) 1 2345678 95; Batch Numbers: 2158303 (Exp. Date: 30 NOV 2022), 2159876 (Exp. Date: 31 JAN 2023), 2156510 (Exp. Date: 30 SEP 2022), 2162996 (Exp. Date: 31 MAR 2023), 2159875 (Exp. Date: 30 NOV 2022), and 2159877 ( Exp. Date: 30 NOV 2022)."
    }
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}