{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Flower Mound",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83510",
      "recalling_firm": "Stryker Communications",
      "address_1": "571 Silveron Blvd",
      "address_2": "N/A",
      "postal_code": "75028",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to CA, CO, CT, FL, GA, IL, IN, MD, MI, MN, MO, NC, NH, NJ, NY, OH, PA, SC, TN, TX, and WI. There was foreign distribution to Canada and Germany.  There was no government/military distribution.",
      "recall_number": "Z-2446-2019",
      "product_description": "Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.",
      "product_quantity": "52 devices",
      "reason_for_recall": "The mounts on the monitor may have an insufficient weld.",
      "recall_initiation_date": "20190801",
      "center_classification_date": "20190830",
      "termination_date": "20210427",
      "report_date": "20190911",
      "code_info": "Serial numbers DFP-075-0307-0001 to DFP-075-1014-0230."
    }
  ]
}