{
  "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,
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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": "15 units",
      "code_info": "Lot Numbers:  23F20A0230  23F20E0004  23F20E0094",
      "center_classification_date": "20210713",
      "distribution_pattern": "US Nationwide distribution in the states of FL, ID, IL, NY, OH, TX.",
      "state": "PA",
      "product_description": "Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr. introducer  Product Code:  AI-07155-IK - 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-2071-2021",
      "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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}