{
  "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": [
    {
      "status": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82865",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:",
      "recall_number": "Z-1800-2019",
      "product_description": "Arrowg+ard Blue Advance JACC\t\t\t\t\t\t\t\t\t\t\t  Product Code:CDC 42052 JX1A",
      "product_quantity": "84 units",
      "reason_for_recall": "Lidstock states the incorrect expiration date for the product",
      "recall_initiation_date": "20190423",
      "center_classification_date": "20190615",
      "termination_date": "20210113",
      "report_date": "20190626",
      "code_info": "Batch Code: 23F18E0046, 23F18J0269"
    }
  ]
}