{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "46926",
      "product_res_number": "Z-0157-2007",
      "event_date_initiated": "2006-06-07",
      "event_date_posted": "2006-11-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-11-13",
      "res_event_number": "35819",
      "product_code": "MGB",
      "pma_numbers": [
        "P930038S040"
      ],
      "product_description": "The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130.  The recalled product is the 6 French model size.",
      "code_info": "Lot 1204437",
      "firm_fei_number": "2182269",
      "recalling_firm": "St. Jude Medical / Daig Division",
      "address_1": "14901 Deveau Pl",
      "city": "Minnetonka",
      "state": "MN",
      "postal_code": "55345-2126",
      "reason_for_recall": "The Angio Seal VIP 6F devices were incorrectly packaged with a 0.038'' guidewire vs. the required 0.035'' guidewire.",
      "root_cause_description": "Other",
      "action": "All consignees were notified by letter on June 7, 2006.  All product is to be retreived by recalling firm''s sales force for return to St. Jude Medical, in Minnetonka, MN.",
      "product_quantity": "4,770 Units",
      "distribution_pattern": "Nationwide.",
      "openfda": {
        "pma_number": [
          "P020035",
          "P040044",
          "P100013",
          "P960043",
          "P930038",
          "P180025",
          "P050043",
          "P210017",
          "P010049",
          "P080029",
          "P230038",
          "P150022",
          "P150006",
          "P920004",
          "P050007",
          "P120016",
          "P040022",
          "P990037"
        ],
        "registration_number": [
          "3013394970",
          "3008307705",
          "3012448339",
          "3002907620",
          "9616099",
          "2024168",
          "2243441",
          "1226183",
          "3002807314",
          "2183744",
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          "3011469355",
          "3015542130",
          "2246552",
          "2029275",
          "3015145497",
          "3008102042",
          "1649518"
        ],
        "fei_number": [
          "3013394970",
          "3002827704",
          "3008307705",
          "3012448339",
          "3001236277",
          "3002907620",
          "2024168",
          "2243441",
          "3010142363",
          "3002807314",
          "3000215205",
          "2183744",
          "3004091615",
          "3012977275",
          "3003898360",
          "1016427",
          "3000215273",
          "3009984513",
          "3005718570",
          "3007766601",
          "2182269",
          "2022435",
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          "1721686",
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          "3015542130",
          "1000306431",
          "2246552",
          "3004635528",
          "3015145497",
          "3002757549",
          "3005747797",
          "3002924544"
        ],
        "device_name": "Device, Hemostasis, Vascular",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}