{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Marketed without a 510K",
      "address_2": "",
      "product_quantity": "4 units",
      "code_info": "Lot Numbers:  16F19J0109",
      "center_classification_date": "20210713",
      "distribution_pattern": "US Nationwide distribution in the states of FL, ID, IL, NY, OH, TX.",
      "state": "PA",
      "product_description": "Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm, Product Code:  AI-07154 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.",
      "report_date": "20210721",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2070-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88120",
      "more_code_info": "",
      "recall_initiation_date": "20210519",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}