{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "66264",
      "product_res_number": "Z-0320-2008",
      "event_date_initiated": "2007-11-09",
      "event_date_posted": "2008-01-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-10-17",
      "res_event_number": "45852",
      "product_code": "HJM",
      "product_description": "Transilluminator, Model BFO-150, a Fiber Optic Light Source (Illuminator), available in 2 voltages: 115v for USA users & 220v for foreign countries. --- Chiu Technical Corporation, 252 Indian Head Road, Kings Park, NY 11754.",
      "code_info": "All Serial Numbers on the market",
      "firm_fei_number": "3001278563",
      "recalling_firm": "Chiu Technical Corp",
      "address_1": "252 Indian Head Road",
      "city": "Kings Park",
      "state": "NY",
      "postal_code": "11754-4818",
      "additional_info_contact": "Mr. Bob Kirzl\n631-544-0606",
      "reason_for_recall": "Device was marketed without a 510(k).",
      "root_cause_description": "Process design",
      "action": "On 11/09/07, the recalling firm started faxing the Recall Letter and response form to its customers, informing them of the recall of the unapproved device to the user level.",
      "product_quantity": "Domestic: 170 units, Foreign: 21 units",
      "distribution_pattern": "Worldwide: USA, Canada and India",
      "openfda": {
        "k_number": [
          "K931072",
          "K893170",
          "K894513",
          "K934269",
          "K972506",
          "K945877",
          "K812949",
          "K950529",
          "K933445",
          "K913273",
          "K940393",
          "K811108"
        ],
        "device_name": "Transilluminator, Ac-Powered",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.1945",
        "device_class": "2",
        "registration_number": [
          "2183446",
          "1000379039",
          "2246552",
          "1423662",
          "2521877",
          "2918630",
          "1315756",
          "2025917",
          "3013002167",
          "1000391004",
          "3016798774",
          "3009106214"
        ],
        "fei_number": [
          "2183446",
          "1000379039",
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}