{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "74618",
      "product_res_number": "Z-0276-2009",
      "event_date_initiated": "2008-09-09",
      "event_date_posted": "2008-11-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-06-02",
      "res_event_number": "50068",
      "product_code": "RHF",
      "product_description": "Barco Surgical Display, Model MDSC-2124\n\nThe 24-inch MDSC-2124 is a near-patient surgical display that uses widescreen (16:10) LCD technology featuring full High Definition resolution (1920 x 1200).  Featuring broad input connectivity, the MDSC-2124 offers a versatile display solution for HD endoscopy cameras, room and boom cameras, ultrasound, PACS and patient information.",
      "code_info": "All lots",
      "firm_fei_number": "3004455125",
      "recalling_firm": "Barcoview",
      "address_1": "35 President Kennedy Park",
      "city": "Kortrijk",
      "country": "Belgium",
      "additional_info_contact": "3256233 Ext. 459",
      "reason_for_recall": "The front protective cover may loosen and completely fall off.",
      "root_cause_description": "Other",
      "action": "Consignees were notified via a Field Safety Notice letter on 09/09/2008. They were instructed to inspect the units to check if the front panel is tightly secured to the display housing. Any front panel found to be lose or showing a gap between the front plate and the back shell of the monitor is to be reported the BARCO Service & Support organization and is to be secured using adhesive tape. Follow up Field Safety Notice was sent to consignees on 09/26/2008 indicating the root cause and the firm's corrective field actions implemented October 15, 2008.",
      "product_quantity": "25 units",
      "distribution_pattern": "Nationwide Distribution --- including states of AK, GA, IL, and MA.",
      "openfda": {
        "device_name": "Digital Display Monitor",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}