{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "94874",
      "product_res_number": "Z-0347-2011",
      "event_date_initiated": "2010-03-15",
      "event_date_posted": "2010-11-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-06-21",
      "res_event_number": "56874",
      "product_code": "LFB",
      "k_numbers": [
        "K982667"
      ],
      "product_description": "SP78100, SP78105\nNasal Products, Catalog Number SP-78100, Nasal Septal Button Standard (3cm), Rx Only, Sterilized by Ethylene Oxide, Micromedics Inc., St Paul, MN 55121-1385.\n\nNasal Products, Catalog Number SP-78105, Nasal Septal Button Oversize (5cm), Rx Only, Sterilized by Ethylene Oxide, Micromedics Inc., St Paul, MN 55121-1385.",
      "code_info": "Model / Lot #: SP78100 / 114149, SP78105 / 114219.",
      "firm_fei_number": "2183425",
      "recalling_firm": "Micromedics, Inc.",
      "address_1": "1270 Eagan Industrial Rd Ste 120 1270 Eagan Industrial Rd",
      "address_2": "Ste 120",
      "city": "Eagan",
      "state": "MN",
      "postal_code": "55121-1385",
      "additional_info_contact": "651-452-1977 Ext. 226",
      "reason_for_recall": "Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.",
      "root_cause_description": "Packaging process control",
      "action": "Micromedics issued a Product Recall letter dated March 15, 2010 to customers, describing the product being recalled, the product sterility issue, and actions to be taken.  The letter advised customers to contact Customer service to return any affected product to Micromedics for replacement.\nCustomers can contact Micromedics at 1-800-624-5662 or 651-452-1977 ext. 226 concerning this recall.",
      "product_quantity": "22",
      "distribution_pattern": "Nationwide Distribution in the states of CA, CT, DE, FL, GA, ID, IL, IN, MD, MA, MI, MN, NJ, NY, NC, PA, TX, UT, and WI.\n\nFRANCE, NETHERLANDS, BELGIUM, UNITED KINGDOM, CANADA, ISRAEL, PERU, SPAIN, IRELAND.",
      "openfda": {
        "device_name": "Button, Nasal Septal",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "U",
        "k_number": [
          "K131745",
          "K862497",
          "K920994",
          "K972060",
          "K013696",
          "K850492",
          "K982667",
          "K781529",
          "K871200",
          "K822637",
          "K871072",
          "K901366"
        ],
        "registration_number": [
          "9612501",
          "1052728",
          "2183762",
          "3017636737",
          "2025182",
          "3008719017",
          "1045254",
          "1926681",
          "1219795",
          "2183744",
          "3018094310",
          "1220850"
        ],
        "fei_number": [
          "2183762",
          "3017636737",
          "2025182",
          "3008719017",
          "1045254",
          "1926681",
          "1219795",
          "3003495548",
          "2183744",
          "3018094310",
          "1220850",
          "1000113735"
        ]
      }
    }
  ]
}