{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Union City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85442",
      "recalling_firm": "Mizuho America, Inc.",
      "address_1": "30057 Ahern Ave",
      "address_2": "N/A",
      "postal_code": "94587-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US: AZ, CA, FL, MO, NC, OH, PA, TX, and WI.  OUS: Greece, Israel, Japan, and Ukraine.",
      "recall_number": "Z-0566-2021",
      "product_description": "Microsurgical Operating Room Tables;7300B (18-350-70);",
      "product_quantity": "8",
      "reason_for_recall": "Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to infrared operating signal errors of Tabletops MST 7300B and MST 7300BX.",
      "recall_initiation_date": "20190911",
      "center_classification_date": "20201214",
      "report_date": "20201223",
      "code_info": "MUC-20168-0001, MUC-20168-0002, MUC-20171-0003, MUC-20171-0004, MUC-20173-0005, MUC-20173-0006, MUC-20178-0007 & MUC-20178-0008"
    }
  ]
}