{
  "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": "2026-04-08",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Athlone",
      "state": "",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79579",
      "recalling_firm": "Teleflex Medical Europe Ltd",
      "address_1": "Ida Business Park",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1370-2018",
      "product_description": "Baker Jejunostomy Tubes:  Product Code   Equivalent Code  (a) 655300160\t  655316  (b) 655500200\t  655520",
      "product_quantity": "200 units",
      "reason_for_recall": "These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.",
      "recall_initiation_date": "20180315",
      "center_classification_date": "20180705",
      "termination_date": "20201005",
      "report_date": "20180418",
      "code_info": "(a) 655300160   655316  Batch Numbers  13EG28  13HG23      (b) 655500200   655520  Batch Numbers:  13EG28",
      "more_code_info": ""
    }
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}