{
  "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": "2026-04-29",
    "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": "65888",
      "recalling_firm": "Stryker Communications",
      "address_1": "1410 Lakeside Pkwy Ste 100",
      "address_2": "N/A",
      "postal_code": "75028-4026",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US natiowide and to the country of Canada.",
      "recall_number": "Z-1992-2013",
      "product_description": "Stryker Visum 300 Ceiling-mounted Exam Light.",
      "product_quantity": "1,375 units",
      "reason_for_recall": "Potential incomplete final weld on the drop tube flange.",
      "recall_initiation_date": "20130725",
      "center_classification_date": "20130821",
      "termination_date": "20150403",
      "report_date": "20130828",
      "code_info": "Product sold under the following part numbers:  0682001410A, 0682001410B, 0682001410C, 0682001410D, 0682001410E, 0682001410F, 0682001410G, and 0682001410H and shipped prior to February 28, 2013."
    }
  ]
}