{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Twinsburg",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88452",
      "recalling_firm": "Hitachi Healthcare Americas Corporation",
      "address_1": "1959 Summit Commerce Park",
      "address_2": "N/A",
      "postal_code": "44087-2371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Mexico and Brazil.",
      "recall_number": "Z-2339-2021",
      "product_description": "OASIS MRI System",
      "product_quantity": "472 (US); 10 (OUS) Total",
      "reason_for_recall": "There was no label on the pad packaging or notification in the user manual that  the table pads contained dry natural rubber which is required by the Code of  Federal Regulations section 21CFR801.437.",
      "recall_initiation_date": "20210729",
      "center_classification_date": "20210824",
      "termination_date": "20230908",
      "report_date": "20210901",
      "code_info": "M001-M329, M951"
    }
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}