{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Bloomington",
      "address_1": "750 N Daniels Way",
      "reason_for_recall": "Label does not state that the product is heparin-coated.",
      "address_2": "",
      "product_quantity": "266",
      "code_info": "Catalog # C-PMS-300-CHILDRENS-A-  032988  ALL LOTS",
      "center_classification_date": "20180309",
      "distribution_pattern": "Nationally",
      "state": "IN",
      "product_description": "Femoral Artery Pressure Monitoring Set",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cook Inc.",
      "recall_number": "Z-0966-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79195",
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      "more_code_info": "",
      "recall_initiation_date": "20171013",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
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