{
  "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-2729-2020",
      "product_description": "Rusch Greenlite Product Code: 004551002  GTIN: 14026704663115 (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": "20600 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:  1906321  1907321  1908321  1909321"
    }
  ]
}