{
  "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": "85996",
      "recalling_firm": "TELEFLEX MEDICAL INC",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.",
      "recall_number": "Z-2731-2020",
      "product_description": "Rusch Greenlite Product Code: 004551004  GTIN: 24026704553796 (each) - Product Usage:   The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.",
      "product_quantity": "350779 units",
      "reason_for_recall": "Breaking at the point of a welded joint",
      "recall_initiation_date": "20200706",
      "center_classification_date": "20200728",
      "termination_date": "20230831",
      "report_date": "20200805",
      "code_info": "Lot/Batch Numbers:  1811341  1901341  1902341  1904341  1905341  1906341  1907341  1908341  1909341"
    }
  ]
}