{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Marketed without a 510K",
      "address_2": "",
      "product_quantity": "48 units",
      "code_info": "Lot Numbers:  16F16F0057 16F19D0027  16F18B0040 16F19E0157  16F18E0121 16F19F0093  16F18F0058 16F19G0066  16F19C0082",
      "center_classification_date": "20210713",
      "distribution_pattern": "US Nationwide distribution in the states of FL, ID, IL, NY, OH, TX.",
      "state": "PA",
      "product_description": "Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm, Product Code: AI-05210 - 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-2068-2021",
      "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"
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}