{
  "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": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84702",
      "recalling_firm": "TELEFLEX MEDICAL INC",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed nationwide in the US and to Puerto Rico; OUS to more than 20 countries; To the following government VA medical Centers:  VAMC - KANSAS CITY MO 4801 E Linwood Blvd Kansas City MO 64128-2218",
      "recall_number": "Z-1117-2020",
      "product_description": "Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System",
      "product_quantity": "338,928 (199,018 US and 139,910 OUS) for all products",
      "reason_for_recall": "The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.",
      "recall_initiation_date": "20200109",
      "center_classification_date": "20200207",
      "termination_date": "20230911",
      "report_date": "20200219",
      "code_info": "Product Code 004551004; Lot Numbers 1812341, 1903341",
      "more_code_info": ""
    }
  ]
}