{
  "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": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80872",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US in the state of PA",
      "recall_number": "Z-3197-2018",
      "product_description": "ARROW¿ Bipolar Electrode Catheter with shrouded pins , 6 Fr, 110 cm  Product Code: AI-06210-S    Product Usage: Arrow electrophysiology catheters are intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording",
      "product_quantity": "7 eaches",
      "reason_for_recall": "Products are labeled with an incorrect expiration date",
      "recall_initiation_date": "20180730",
      "center_classification_date": "20180919",
      "termination_date": "20190711",
      "report_date": "20180926",
      "code_info": "Lot/Batch Number:16F18A0010  Use By: 2023-12-31"
    }
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}