{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  "results": [
    {
      "cfres_id": "31412",
      "product_res_number": "Z-0589-04",
      "event_date_initiated": "2004-02-19",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-01-25",
      "res_event_number": "28229",
      "product_code": "KZF",
      "k_numbers": [
        "K851742"
      ],
      "product_description": "All Outpatient and Coolspot single ceiling or single track Medical Examination Lights manufactured before August 2000. Products manufactured during or after August 2000 contain a redesigned pivot assembly and are not included in this recall. Affected products include:\n\nModel 100540  Fleximount SGL Ceiling, Serial No.''s less than SC995486\nModel 100740 SGL Ceiling CS II, Serial No''s less than SCCS990745\nModel 100580 SGL Trolley, Serial No.''s less than TRS962633\nModel 100780 SGL Trolley OP II, Serial No.''s less than STOP97417\nModel 102540 SGL Ceiling OP II, Serial No.''s less than SCOP003354.",
      "code_info": "See Product Description",
      "firm_fei_number": "2018492",
      "recalling_firm": "Burton Medical Products Corp",
      "address_1": "21100 Lassen St",
      "city": "Chatsworth",
      "state": "CA",
      "postal_code": "91311-4250",
      "additional_info_contact": "Sharon Anderson\n800-444-9909 Ext. 164",
      "reason_for_recall": "Pivot joint on these ceiling mount lights may fail and lights may fall onto patients.",
      "root_cause_description": "Component design/selection",
      "action": "Firm will ask for subdistribution information from thier distributors via letter on 1/30/2004. Letters will be sent directly to users. Firm will retrofit all sites with suspect units with new pivot assemblies.",
      "product_quantity": "17,000 estimated",
      "distribution_pattern": "Nationwide.",
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        "device_name": "Device, Medical Examination, Ac Powered",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6320",
        "device_class": "1"
      }
    }
  ]
}