{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dublin",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93506",
      "recalling_firm": "Smiths Medical Asd Inc",
      "address_1": "6250 Shier Rings Rd",
      "address_2": "N/A",
      "postal_code": "43016-1270",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, UAE.",
      "recall_number": "Z-0745-2024",
      "product_description": "20IN (50.8CM) BRAIDED INJ LINE, ROTATING ADAPT,  List Number MX682BR",
      "product_quantity": "31,685 total",
      "reason_for_recall": "There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the device\u0019s O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication which may potentially lead to under infusion of medication.",
      "recall_initiation_date": "20231110",
      "center_classification_date": "20240117",
      "report_date": "20240124",
      "code_info": "Lot Number: 4398428 4404690"
    }
  ]
}