{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "49777",
      "product_res_number": "Z-0394-2007",
      "event_date_initiated": "2006-12-20",
      "event_date_posted": "2007-02-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-10-23",
      "res_event_number": "37021",
      "product_code": "DTK",
      "k_numbers": [
        "K052578"
      ],
      "product_description": "Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism.  Catalog Number RF-220J  ***For Canada & Australia only***",
      "code_info": "Lot numbers: GFPK3279, GFPK3280, GFPK3281 & GFPK3282",
      "firm_fei_number": "2020394",
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "address_1": "1625 W 3rd St",
      "city": "Tempe",
      "state": "AZ",
      "postal_code": "85281-2438",
      "additional_info_contact": "Shari L. Allen, RAC\n480-303-2720",
      "reason_for_recall": "This action is being taken because BPV has recently received three complaints for the device that involve reports of introducer sheath tip damage.  The damage may result in loss of tip integrity.",
      "root_cause_description": "Other",
      "action": "Recall letters were sent to all consignees via Federal Express overnight delivery with signature receipt required on  December 20, 2006. Each letter included a Recall and Effectiveness Check Form for each consignee to fill out and fax to Bard Peripheral Vascular, Inc (BPV). Customers will be asked to immediately remove product from inventory and isolated from use and contact BARD for return authorization.  All returned product will be destroyed.",
      "product_quantity": "124 units",
      "distribution_pattern": "Worldwide including USA, Australia, and Canada",
      "openfda": {
        "k_number": [
          "K171712",
          "K870729",
          "K964284",
          "K150262",
          "K172584",
          "K241507",
          "K093659",
          "K925679",
          "K032426",
          "K031328",
          "K912035",
          "K122585",
          "K760152",
          "K010083",
          "K091077",
          "K874096",
          "K121629",
          "K130366",
          "K963014",
          "K852097",
          "K211874",
          "K090140",
          "K061815",
          "K211875",
          "K163699",
          "K062887",
          "K940489",
          "K233680",
          "K112119",
          "K771046",
          "K242612",
          "K162875",
          "K023116",
          "K080668",
          "K172557",
          "K944353",
          "K070514",
          "K000855",
          "K912144",
          "K120402",
          "K901454",
          "K022236",
          "K143208",
          "K052578",
          "K073090",
          "K000062",
          "K970099",
          "K082305",
          "K081410",
          "K050558",
          "K112497",
          "K901235",
          "K133243",
          "K073528",
          "K063217",
          "K010485",
          "K073374",
          "K101431",
          "K901659",
          "K963016",
          "K881604",
          "K160866",
          "K043509",
          "K140286",
          "K152765",
          "K932921",
          "K894703",
          "K181202",
          "K951508",
          "K113124",
          "K003964",
          "K240257",
          "K072240",
          "K955396",
          "K240578",
          "K760151",
          "K161218",
          "K102511",
          "K034050",
          "K121057",
          "K143405",
          "K081138",
          "K173236"
        ],
        "pma_number": [
          "P850049"
        ],
        "registration_number": [
          "1018233",
          "1721686",
          "3007156625",
          "1313046",
          "1643817",
          "3009888344",
          "3002808486",
          "3004111573",
          "3005580113",
          "3006082230",
          "1016427",
          "3013764800",
          "9616099",
          "9612452",
          "3009526575",
          "3007080617",
          "2020394",
          "1722746",
          "3002807314",
          "3010383847",
          "1625425",
          "1820334"
        ],
        "fei_number": [
          "1018233",
          "1721686",
          "1313046",
          "1643817",
          "3009888344",
          "3002808486",
          "3002806713",
          "3003528016",
          "3004111573",
          "3005580113",
          "3006082230",
          "1016427",
          "3013764800",
          "3009526575",
          "1000306216",
          "3007080617",
          "2020394",
          "3002807314",
          "3010383847",
          "1625425",
          "3008133910",
          "1820334"
        ],
        "device_name": "Filter, Intravascular, Cardiovascular",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.3375",
        "device_class": "2"
      }
    }
  ]
}