{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84520",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: FL",
      "recall_number": "Z-0837-2020",
      "product_description": "Arrow Endurance\" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH",
      "product_quantity": "575",
      "reason_for_recall": "Potential sterility issue for specific lots of  the Arrow Endurance\" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.",
      "recall_initiation_date": "20191206",
      "center_classification_date": "20200122",
      "termination_date": "20211102",
      "report_date": "20200129",
      "code_info": "REF: ASK-00820-FLH  Manufacturing Lots: 13F19E0247, 13F19F0006, and 13F19G0433  Exp. Date: Aug. 2020 - Sep. 2020",
      "more_code_info": ""
    }
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}