{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
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  "results": [
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      "cfres_id": "159075",
      "product_res_number": "Z-0098-2018",
      "event_date_initiated": "2017-10-10",
      "event_date_created": "2017-11-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-06-22",
      "res_event_number": "78289",
      "product_code": "NKC",
      "product_description": "STORZ High Flow Insufflation Tubing (with filter), Catalog #20400161S/10 (outer box label), ENDOFLATOR 26-430520-1 also referenced on outer box), individually packaged in a sterile pouch (Catalog #20400161S), 10 pouches per cardboard box.  Some of the pouches inside of cardboard box are incorrectly labeled as Catalog number 20400162S, High Flow Insufflation Tubing (with filter) For 26432020-1 THERMOFLATOR.  The firm name on the label is Karl Storz Endoscopy-America, Inc., El Segundo, CA.",
      "code_info": "Lot #129241",
      "firm_fei_number": "3007475226",
      "recalling_firm": "Karl Storz Endoscopy",
      "address_1": "2151 E Grand Ave",
      "city": "El Segundo",
      "state": "CA",
      "postal_code": "90245-5017",
      "additional_info_contact": "Susie S. Chen\n424-218-8201",
      "reason_for_recall": "The label outside the cardboard box is labeled correctly but the pouches inside of some of the boxes were mislabeled as a different product.",
      "root_cause_description": "Labeling mix-ups",
      "action": "The recalling firm issued letters flagged as 'SAFETY ALERT\" dated 10/5/2017 via Federal Express on 10/10/2017.",
      "product_quantity": "496/10-pouch boxes",
      "distribution_pattern": "Distribution was made nationwide.  There was government distribution and no military distribution.  Foreign distribution was made to Canada.",
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        "device_name": "Tubing/Tubing With Filter, Insufflation, Laparoscopic",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.1730",
        "device_class": "1"
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}