{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91077",
      "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 Nationwide distribution.",
      "recall_number": "Z-0274-2023",
      "product_description": "BASIN SET, MEBS42K, general surgical kit",
      "product_quantity": "1504 trays",
      "reason_for_recall": "Basin Set labeling error:  components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.",
      "recall_initiation_date": "20221012",
      "center_classification_date": "20221122",
      "termination_date": "20250306",
      "report_date": "20221130",
      "code_info": "UDI/DI 00191072151742, Batch/Lot No. 833221, exp 6/16/2023"
    }
  ]
}