{
  "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": "43257",
      "product_res_number": "Z-0467-06",
      "event_date_initiated": "2005-11-17",
      "event_date_posted": "2006-02-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-03-03",
      "res_event_number": "34199",
      "product_code": "GCD",
      "k_numbers": [
        "K850505"
      ],
      "product_description": "BD Perisafe catheter with catheter connector.  The catheter connector has four components:  body (green), cap (white), washer (white), and gasket (grey).   It is used for continuous administration of anesthesia.  The product is molded and assembled by Avail, Northeast.  It is then supplied to BD (Juncos, PR) where it is allocated to be packaged and sold in kits, trays, Perisafe and bulk.",
      "code_info": "Reorder Number 400507 Lot Number 5222801.",
      "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": "Greg Morgan\n201-847-4344",
      "reason_for_recall": "The catheter connector could not be sufficiently tightened to secure the catheter tubing.",
      "root_cause_description": "Other",
      "action": "Recall letters were sent to all direct consignees and potential end users of the product on 11/17/2005.  Letters were mailed via UPS second day air.",
      "product_quantity": "1410 units",
      "distribution_pattern": "The devices were distributed to wholesalers and hospitals nationwide.  There are no international or govt accounts.",
      "openfda": {
        "k_number": [
          "K863446",
          "K851196",
          "K851921",
          "K760203",
          "K760524",
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        ],
        "device_name": "Connector, Catheter",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4200",
        "device_class": "1"
      }
    }
  ]
}