{
  "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": [
    {
      "country": "United States",
      "city": "Flower Mound",
      "address_1": "571 Silveron Blvd",
      "reason_for_recall": "The back cover of the light head was insufficiently assembled and could potentially fall off the light.",
      "address_2": "",
      "product_quantity": "3,344 lights",
      "code_info": "Serial number ranges: 83171-0017818 to 83171-0123938",
      "center_classification_date": "20190912",
      "distribution_pattern": "Distribution was nationwide, including to Puerto Rico.  There was also government/military distribution.    Foreign distribution was made to Argentina, Austria, Australia, Belgium, Bulgaria, Canada, China, Colombia, Denmark, France, Germany, Hong Kong, India, Indonesia, Italy, Japan, Kazakhstan, Korea, Kuwait, Lithuania, Mexico, Netherlands, Philippines, Poland, Russia, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Taiwan, United Arab Emirates, United Kingdom, Uruguay, and Vietnam.",
      "state": "TX",
      "product_description": "Berchtold Chromophare F628 Surgical Lights.    Product Usage:    The medical lights are for usage in hospital treatment rooms. They provide localized lighting focused on the patient s body for detecting and treating disease, injury, and disability. The surgical lights may only be used in rooms used for medical purposes that have been equipped in accordance with VDE 0100-710 or IEC 60364-7-10 in accordance with the regulations.",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Communications",
      "recall_number": "Z-2540-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83355",
      "more_code_info": "",
      "recall_initiation_date": "20190322",
      "postal_code": "75028",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}