{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Harlan",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64471",
      "recalling_firm": "Molded Products Inc",
      "address_1": "1112 Chatburn Ave",
      "address_2": "N/A",
      "postal_code": "51537-2007",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to one customer in Michigan.",
      "recall_number": "Z-0969-2013",
      "product_description": "Sterile Access & Return Line Set, 36\" Length, Part # UM-872-36.      Intended for use with medically prescribed hemodialysis blood tubing.",
      "product_quantity": "1200 sets",
      "reason_for_recall": "The recalled product leaks at the connection site.",
      "recall_initiation_date": "20120619",
      "center_classification_date": "20130318",
      "termination_date": "20130814",
      "report_date": "20130327",
      "code_info": "Lot numbers:  80106 and 80106b"
    }
  ]
}