{
  "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,
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    {
      "status": "Ongoing",
      "city": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89868",
      "recalling_firm": "American Contract Systems, Inc.",
      "address_1": "2610 Ne Industrial Dr Ste 220",
      "address_2": "N/A",
      "postal_code": "64117-2648",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of IL, MO, NE, and TX.",
      "recall_number": "Z-1040-2022",
      "product_description": "ACS Cath Lab Pack",
      "product_quantity": "10 packs",
      "reason_for_recall": "Product was sterilized with a higher than specification EO concentration.",
      "recall_initiation_date": "20220322",
      "center_classification_date": "20220506",
      "report_date": "20220518",
      "code_info": "Model FTCL83K, Lot 982221  UDI: 00191072151360"
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}