{
  "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": {
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  "results": [
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      "status": "Ongoing",
      "city": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92240",
      "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": "E-Mail",
      "distribution_pattern": "US Distribution to the state of:  MA",
      "recall_number": "Z-1973-2023",
      "product_description": "Total Knee Pack, REF CETJ130, medical convenience kits",
      "product_quantity": "36 units",
      "reason_for_recall": "Incorrect expiration date on product.",
      "recall_initiation_date": "20230417",
      "center_classification_date": "20230615",
      "report_date": "20230621",
      "code_info": "UDI/DI: 00191072179593; Lot Number: 967231"
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}