{
  "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": "36787",
      "product_res_number": "Z-0437-05",
      "event_date_initiated": "2005-01-12",
      "event_date_posted": "2005-01-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-02-09",
      "res_event_number": "30903",
      "product_code": "NIQ",
      "pma_numbers": [
        "P020026"
      ],
      "product_description": "Polymeric coated stent.  Cypher BX Velocity Cardio Sirolimus Stents.",
      "code_info": "Lot no. X1004212",
      "firm_fei_number": "1016427",
      "recalling_firm": "Cordis Corporation",
      "address_1": "14201 NW 60th Ave",
      "city": "Miami Lakes",
      "state": "FL",
      "postal_code": "33014-2802",
      "reason_for_recall": "Six of 370 stents released to market had a slightly below the required polymeric coating weight.  All other specification were met.",
      "root_cause_description": "Other",
      "action": "A withdrawal letter is in the process of being hand-delivered to accounts that received this lot, by a Cordis sales representative.  Any remaining units from this lot are being removed, and returned to Cordis.  The returned units will be scrapped.  An Acknowledgement Form is being signed  indicating that the account was informed, and documenting whether there is any remaining product from this lot.  The withdrawal action was initiated January 12, 2005.",
      "product_quantity": "300",
      "distribution_pattern": "Distributed throughout the United States.",
      "openfda": {
        "pma_number": [
          "P110019",
          "P030025",
          "P190020",
          "P020026",
          "P100023",
          "P110010",
          "P950020",
          "P060033",
          "P170030",
          "P160043",
          "P170008",
          "P110013",
          "P150003",
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        ],
        "device_name": "Coronary Drug-Eluting Stent",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}