{
  "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": "25424",
      "product_res_number": "Z-0352-03",
      "event_date_initiated": "2002-12-11",
      "event_date_created": "2015-06-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-05-28",
      "res_event_number": "25226",
      "product_code": "79F",
      "k_numbers": [
        "K002233"
      ],
      "product_description": "Surgical Mesh",
      "code_info": "lot number 547628",
      "firm_fei_number": "2183620",
      "recalling_firm": "Synovis Surgical Inovation       Div. of",
      "address_1": "2575 University Ave.",
      "city": "St. Paul",
      "state": "MN",
      "postal_code": "55114-1024",
      "reason_for_recall": "A gap in the exterior seal may lead to sterility concerns with the interior pouch.",
      "root_cause_description": "Other",
      "action": "The sites and/or distributors that received suspect devices were contacted by telephone on 12/11/02 and given instructions on how to return/replace the devices.  In addition, a letter dated 12/11/02 was sent to each consignee.",
      "product_quantity": "28 devices",
      "distribution_pattern": "Product shipped nationwide, no foreign consignees",
      "openfda": {}
    }
  ]
}