{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "49987",
      "product_res_number": "Z-0526-2007",
      "event_date_initiated": "2007-01-08",
      "event_date_posted": "2007-02-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-11-18",
      "res_event_number": "37120",
      "product_code": "FTD",
      "k_numbers": [
        "K915285"
      ],
      "product_description": "Skytron Infinity Series surgical light, 4 bulbs in 1 - 22' diameter lighthead, Manufactured by Dai-ichi Shomei Co., Ltd., Made in Japan; Models IF54, IF54EL, IF54LH and IF54S.",
      "code_info": "Each lighthead bears a unique serial number.  For units with model numbers beginning in IF54, all serial numbers with the following numbers in the third and fourth positions of the numerical series:  95, 96, 97, 98, 99, 00 or 01 (example: xx98xxx).",
      "firm_fei_number": "1825014",
      "recalling_firm": "Skytron, Div. The KMW Group, Inc",
      "address_1": "5000 36th St Se",
      "city": "Grand Rapids",
      "state": "MI",
      "postal_code": "49512-2008",
      "additional_info_contact": "Mary Preston-Murphy\n800-759-8766 Ext. 3048",
      "reason_for_recall": "If the mounting plug is improperly adjusted, the unit could separate, come apart, and fall from the mount.",
      "root_cause_description": "Other",
      "action": "The firm initially notified consignees of this problem on 11/23/1999 and again on 11/01/2002 and most lights have already been corrected.  Remaining consignees with lights in need of correction were notified of the problem via letter dated 1/8/07 and instructed to contact the distributor to have their lights inspected and modified.",
      "product_quantity": "5,000 for all models.",
      "distribution_pattern": "Nationwide and Canada.",
      "openfda": {
        "k_number": [
          "K932451",
          "K003423",
          "K133425",
          "K770568",
          "K041681",
          "K823360",
          "K123776",
          "K053364",
          "K961122",
          "K801353",
          "K841360",
          "K931675",
          "K770861",
          "K130513",
          "K930897",
          "K100884",
          "K981717",
          "K111020",
          "K942553",
          "K811728",
          "K071180",
          "K010724",
          "K770567",
          "K895715",
          "K954263",
          "K100234",
          "K013242",
          "K882613",
          "K860088"
        ],
        "registration_number": [
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          "3009715914",
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        "fei_number": [
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          "3007513035",
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          "1037039",
          "3005747797",
          "3023530182",
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          "3008716327",
          "3009905888",
          "3016904853",
          "3027847726",
          "2648666",
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          "3002732397",
          "3003184737",
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          "3002807830",
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        ],
        "device_name": "Lamp, Surgical",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4580",
        "device_class": "2"
      }
    }
  ]
}