{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "104880",
      "product_res_number": "Z-0174-2012",
      "event_date_initiated": "2011-06-15",
      "event_date_posted": "2011-11-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-07-27",
      "res_event_number": "60255",
      "product_code": "KZH",
      "k_numbers": [
        "K024112"
      ],
      "product_description": "1.0mL 28 G x 1/2\" blister packaged insulin syringe Catalog Number 329424; Lot Number 0039920\n\nIntended use: Subcutaneous injection of insulin.",
      "code_info": "K024112 D039612 Catalog Number 329424 Lot Number 0039920",
      "firm_fei_number": "2243072",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "city": "Franklin Lakes",
      "state": "NJ",
      "postal_code": "07417-1815",
      "additional_info_contact": "Ms. Yogindra Dellow\n201-847-5033",
      "reason_for_recall": "Experiment labels may be on shelf cartons of 1.0ml 28G x 1/2 blister packaged insulin syringes.",
      "root_cause_description": "Labeling mix-ups",
      "action": "The firm, BD, sent an \"PRODUCT RECALL NOTIFICATION\" letter and response form dated June 15, 2011 to their consignee/customers. The letter describes the product, problem and actions to be taken.  The customers were instructed to immediately review their inventory for the affected product, remove the product from inventory, quarantine the product and return it to BD; if the product was further distributed,  they should identify their customers and notify them at once, and complete and return the attached Tracking/Verification Form via fax to: 201-847-4853.\n\nIf you have any questions, contact Customer Service at 1-800-237-2762, Monday -Thursday, 8:00am-6:30pm and on Friday, 8:00-5:30pm Eastern Standard Time.",
      "product_quantity": "10,230 shelf cartons (1,0230,000 syringes)",
      "distribution_pattern": "Nationwide Distribution.",
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        "k_number": [
          "K013362",
          "K860284",
          "K954729",
          "K073476",
          "K060389",
          "K000482",
          "K883164",
          "K033696",
          "K981266",
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          "K993385",
          "K141384",
          "K834440",
          "K243232",
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          "K042557",
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          "K862325",
          "K790104",
          "K945473",
          "K961309",
          "K992300",
          "K163400"
        ],
        "device_name": "Introducer, Syringe Needle",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6920",
        "device_class": "2",
        "registration_number": [
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}