{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sanford",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93123",
      "recalling_firm": "Omega Medical Imaging, Inc.",
      "address_1": "3400 Saint Johns Pkwy Ste 1020",
      "address_2": "N/A",
      "postal_code": "32771-6769",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Alabama, California, Illinois, Indiana, Kentucky, Louisiana, Missouri, Montana, North Carolina, Ohio, Oklahoma",
      "recall_number": "Z-0160-2024",
      "product_description": "Omega Medical Imaging Elevating Monitor Suspension Systems, Part Number 1000-0085",
      "product_quantity": "31 units",
      "reason_for_recall": "An actuator separated from the pivot mechanism on a lower monitor boom system column. The lower boom became detached at the point shown and was restrained by the installed safety cable.",
      "recall_initiation_date": "20230908",
      "center_classification_date": "20231024",
      "report_date": "20231101",
      "code_info": "all units manufactured between 10-22-2012 and 07-09-2019"
    }
  ]
}