{
  "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,
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  "results": [
    {
      "cfres_id": "114097",
      "product_res_number": "Z-0402-2013",
      "event_date_initiated": "2011-11-17",
      "event_date_posted": "2012-11-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-11-20",
      "res_event_number": "63512",
      "product_code": "EBA",
      "product_description": "Freedom Cordless LED Light System. Freedom System, Standard Length, Part Number 910863-1, Serial Numbers 77001000-77003470 and Freedom System, Long Length, Part Number 910863-2, Serial Numbers 77001000-77003470.\n\nFreedom Cordless LED Light System is a Class I Medical Device. The device\nlisting number this product is E115952.\n\nThe intended use of this device is to illuminate oral structures and operating areas.",
      "code_info": "Freedom System, Standard Length, Part Number 910863-1, Serial Numbers 77001000-77003470 and Freedom System, Long Length, Part Number 910863-2, Serial Numbers 77001000-77003470.   Freedom Cordless LED Light System has no expiration date. The affected units were produced and distributed since February 2011.",
      "firm_fei_number": "3003848022",
      "recalling_firm": "Kerr Corporation",
      "address_1": "3225 Deming Way",
      "city": "Middleton",
      "state": "WI",
      "postal_code": "53562",
      "additional_info_contact": "608-831-2555",
      "reason_for_recall": "The firm recalled the Freedom Cordless LED Headlight because some units were assembled with an incorrect component in the\ncontrol board electronics that may cause some Freedom Cordless LED Headlight units to become warm to the touch; however, no skin damage will occur.",
      "root_cause_description": "Labeling mix-ups",
      "action": "Orascoptic sent an \"URGENT: MEDICAL DEVICE RECALL\" letter dated November 17, 2011.  The letter identified the product, problem, and actions to be taken by the customers. An Acknowledgement Form was included for customers to complete and return to the firm. Contact Orascoptic Customer Care at 608-831-2555 for assistance regarding this notice.",
      "product_quantity": "1330 units",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Canada, Australia, and Europe.",
      "openfda": {
        "k_number": [
          "K790806",
          "K923949",
          "K842358",
          "K893458",
          "K854646",
          "K790807",
          "K070287",
          "K810117",
          "K842515",
          "K822265"
        ],
        "device_name": "Light, Surgical Headlight",
        "medical_specialty_description": "Dental",
        "regulation_number": "872.4630",
        "device_class": "1",
        "registration_number": [
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