{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Sanford",
      "address_1": "675 Hickman Cir",
      "reason_for_recall": "Elevating Monitor Suspension separated from the lifting column bracket",
      "address_2": "",
      "product_quantity": "26 units",
      "code_info": "Model:  Elevating Monitor Suuspension P/Ns:  1000-0085, 1000-0095 and (1000-0129 one unit produced does not use bracket 1040-0071 or 1040-0031).",
      "center_classification_date": "20160903",
      "distribution_pattern": "CO, MN, GA, NC, IN, OH, KY, IL, NY, AL, MO, LA, PA, and SD Denmark",
      "state": "FL",
      "product_description": "2 over 2 Elevating Monitor Suspension  - Omega Medical Imaging, LLC Elevating Monitor Suspension Systems.",
      "report_date": "20160914",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Omega Medical Imaging, Inc.",
      "recall_number": "Z-2734-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74886",
      "termination_date": "20191004",
      "more_code_info": "",
      "recall_initiation_date": "20160621",
      "postal_code": "32771-6931",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}