{
  "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": "174932",
      "product_res_number": "Z-0407-2020",
      "event_date_initiated": "2019-06-24",
      "event_date_created": "2019-11-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-07-24",
      "res_event_number": "83359",
      "product_code": "OGR",
      "product_description": "EPISTAXIS TRAY\nKit Code: MNS10165",
      "code_info": "Lot # 2019051350  Exp 08/31/2020 Lot # 2019021501  Exp 04/30/2020 Lot # 2019010701  Exp 04/30/2020 Lot # 2018112601  Exp 04/30/2020 Lot # 2018092501  Exp 09/30/2019 Lot # 2018100201  Exp 09/30/2019 Lot # 2018062801  Exp 12/31/2019 Lot # 2018073101  Exp 09/30/2019 Lot # 2018042701  Exp 02/28/2019",
      "firm_fei_number": "3008403546",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "100 Centurion Way",
      "city": "Williamston",
      "state": "MI",
      "postal_code": "48895-9086",
      "additional_info_contact": "Lisa A. Carpenter\n517-546-5400 Ext. 1156",
      "reason_for_recall": "Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer",
      "root_cause_description": "Material/Component Contamination",
      "action": "1. Please identify all inventory that you have within your possession. Remove the MAJOR Nasal Decongestant from the mini-grip bag and segregate it in a location where it cannot be accessed for use.\n2. Please complete the enclosed accountability record, whether or not you have product, and fax or email at your earliest convenience to the attention of Lisa Carpenter as directed.  Upon receipt of this recall response, a Centurion Representative will contact you regarding retrieval of the product from your facility, if required.\n3. please forward a copy of this notice to any facilities to whom this product may have been further distributed.\n\nIf you have any questions, please contact (517) 546-5400 Ext 1122.",
      "product_quantity": "525 Kits",
      "distribution_pattern": "CT, IL",
      "openfda": {
        "device_name": "Ear, Nose, And Throat Surgical Tray",
        "medical_specialty_description": "Ear, Nose, Throat",
        "regulation_number": "874.4420",
        "device_class": "1",
        "registration_number": [
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