{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "43269",
      "product_res_number": "Z-0372-06",
      "event_date_initiated": "2005-12-01",
      "event_date_posted": "2006-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-04-30",
      "res_event_number": "34204",
      "product_code": "KSR",
      "k_numbers": [
        "K011984"
      ],
      "product_description": "BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder.",
      "code_info": "Catalog # -- Lot #:  367352 -- 5188576; 367352 -- 5208448; 367352 -- 5217290; 368656 -- 5164491; 368656 -- 5164526; 368656 -- 5187894; 368656 -- 5192496; 368656 -- 5220204; 368656 -- 5238936.",
      "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": "Kevin Nolan\n201-847-5651",
      "reason_for_recall": "Cracked finger grip luer adapter components on the Push Button Blood Collection Set.",
      "root_cause_description": "Other",
      "action": "Recall notification was sent out to the customers on 12/5/2005.",
      "product_quantity": "118200 each",
      "distribution_pattern": "The device was shipped to 23 wholesalers,  5 hospitals, and 1 VA govt. account nationwide.",
      "openfda": {
        "k_number": [
          "K780354",
          "K801219",
          "K032827",
          "K791673",
          "K792395",
          "K810500",
          "K801082",
          "K760952",
          "K810897",
          "K781811",
          "K811523",
          "K810313",
          "K811449",
          "K792185",
          "K810711",
          "K020753"
        ],
        "registration_number": [
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        "fei_number": [
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        ],
        "device_name": "Container, Empty, For Collection & Processing Of Blood & Blood Components",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.9100",
        "device_class": "2"
      }
    }
  ]
}