{
  "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": "2026-08-13",
    "results": {
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    {
      "cfres_id": "140795",
      "product_res_number": "Z-0161-2016",
      "event_date_initiated": "2015-08-13",
      "event_date_posted": "2015-10-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2017-10-13",
      "res_event_number": "72365",
      "product_code": "LLB",
      "k_numbers": [
        "K071145"
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      "product_description": "Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring an extracorporeal circuit of larger volumes of blood.",
      "code_info": "Lot # 15C03",
      "firm_fei_number": "1000132332",
      "recalling_firm": "Nipro Medical Corporation",
      "address_1": "3150 Nw 107th Ave",
      "city": "Miami",
      "state": "FL",
      "postal_code": "33172",
      "additional_info_contact": "Jessica Oswald -McLeod\n305-599-7174",
      "reason_for_recall": "Some 1 1/4\" needles were packaged and labeled in the 1\" blister package.",
      "root_cause_description": "Mixed-up of materials/components",
      "action": "Customers were issued a RMA 60001203 on August 18, 2015.",
      "product_quantity": "50,000 pieces",
      "distribution_pattern": "Indiana",
      "openfda": {
        "device_name": "System, Blood, Extracorporeal And Accessories",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5820",
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