{
  "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": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Shipping carton labeling error.",
      "address_2": "",
      "product_quantity": "690 kits",
      "code_info": "Device Listing # D025180",
      "center_classification_date": "20160907",
      "distribution_pattern": "Nationwide Distribution to OH, IN, TN, NC, and KY.",
      "state": "PA",
      "product_description": "Radial Artery Catheterization Kit with Sharps Safety Features  Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.",
      "report_date": "20160914",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2741-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74986",
      "termination_date": "20170822",
      "more_code_info": "",
      "recall_initiation_date": "20160808",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}