{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Warwick",
      "state": "RI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91564",
      "recalling_firm": "Unetixs Vascular, Inc.",
      "address_1": "333 Strawberry Field Rd Ste 11",
      "address_2": "N/A",
      "postal_code": "02886-2459",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and Global distribution.",
      "recall_number": "Z-1194-2023",
      "product_description": "MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01",
      "product_quantity": "2310 units",
      "reason_for_recall": "The current luer fittings and adaptors allow for the possibility of the air line to be misconnected to an intravenous line, which may cause an air embolism.",
      "recall_initiation_date": "20230210",
      "center_classification_date": "20230301",
      "report_date": "20230308",
      "code_info": "All Serial Numbers",
      "more_code_info": ""
    }
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}