{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 7
    }
  },
  "results": [
    {
      "cfres_id": "103036",
      "product_res_number": "Z-0073-2012",
      "event_date_initiated": "2011-07-29",
      "event_date_posted": "2011-10-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-08-27",
      "res_event_number": "59536",
      "product_code": "JEA",
      "k_numbers": [
        "K910736"
      ],
      "product_description": "Mizuho OSI Modular Table System;\n\n\nProduct Usage:  For use in orthopaedic surgery to provide support to a patient.",
      "code_info": "Model numbers 5803, 5855, 5890, 5891, 5892, 5895, 5927, 5840-726, 5840-831, 5943, 5843A, 5996, 5996I and 6977.; all codes Mizuho OSI, 30031 Ahern Ave., Union City, CA 94587",
      "firm_fei_number": "2921578",
      "recalling_firm": "Mizuho Orthopedic Systems Inc",
      "address_1": "30031 Ahern Ave",
      "city": "Union City",
      "state": "CA",
      "postal_code": "94587",
      "additional_info_contact": "Kirke Jayne\n510-476-8128",
      "reason_for_recall": "Reports of injury related incidents while using the Mizuho OSI Modular Table System.",
      "root_cause_description": "Use error",
      "action": "Mizuho Orthopedic Systems Inc sent a \"Field Advisory Notice (Recall)\" letters dated July 29, 2011 to all customers using the Modular Table System via Federal Express.  The Field Advisory Notice reference the devices involved and explain that there is no need to return any product or to discontinue the use.  The letter provides WARNINGS and RECOMMENDATIONS for all users to consider when using the devices and request that the response form be completed as instructed in the advisory communication.  The letters also recommend that awareness, training, inspection prior to use, and proper maintenance be established and practiced.  The letter recommend that the Field Advisory Notices be posted in prominent areas and communicated to all staff and potential users of this device.  Additional support and training can be obtained by contacting Mizuho OSI's Customer Resource Group at 1-800-777-4674.  For further questions concerning this notification, contact the Director of Customer Resource Group for assistance (1-800-777-4674, outside the USA 00+1-510-476-8199).\nRevised letters were approved by CDRH and sent out in January 2012.",
      "product_quantity": "15,011 units",
      "distribution_pattern": "Worldwide Distribution - Nationwide USA",
      "openfda": {
        "registration_number": [
          "3012995405",
          "9681642",
          "3010890274",
          "2221819",
          "3013522950",
          "1043572",
          "3007031002",
          "2916273",
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          "8010652",
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          "3009760038",
          "3013836619",
          "3015223105",
          "3011111237"
        ],
        "fei_number": [
          "1841",
          "3012995405",
          "1000295034",
          "3010890274",
          "2221819",
          "3013522950",
          "1043572",
          "3007031002",
          "2916273",
          "2921578",
          "3003184737",
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          "1000351276",
          "3031563141",
          "3012329926",
          "3007143268",
          "3027847726",
          "3009760038",
          "3013836619",
          "3002619595",
          "3015223105",
          "3011111237"
        ],
        "device_name": "Table, Surgical With Orthopedic Accessories, Ac-Powered",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4960",
        "device_class": "1",
        "k_number": [
          "K900290",
          "K873079",
          "K953071",
          "K881060",
          "K873080",
          "K924094",
          "K894789",
          "K910736",
          "K911522",
          "K874762"
        ]
      }
    }
  ]
}