{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Research Triangle Park",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78929",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2917 Weck Dr",
      "address_2": "N/A",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US only",
      "recall_number": "Z-0705-2018",
      "product_description": "Rusch Greenlite MAC 1, Catalog Number 004551001.  Used during tracheal intubation.",
      "product_quantity": "2140 units",
      "reason_for_recall": "The pouch may contain the incorrect Rusch  Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may  instead contain RUSCH GREEN LITE MAC 2.",
      "recall_initiation_date": "20170110",
      "center_classification_date": "20180223",
      "termination_date": "20210413",
      "report_date": "20180307",
      "code_info": "Lot/Serial number:  1602312"
    }
  ]
}