{
  "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": "175684",
      "product_res_number": "Z-0256-2020",
      "event_date_initiated": "2019-07-15",
      "event_date_created": "2019-10-31",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-08-31",
      "res_event_number": "83542",
      "product_code": "OXQ",
      "product_description": "PORT ACCESS INFUSION KIT - 1\" NEEDLE\nProduct Code: DYNDC2817",
      "code_info": "Lot Number      Expiration 2019060390\t11/30/2020",
      "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\n517-545-1156",
      "reason_for_recall": "Supplier initiated recall  of the GRIPPER Needles",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "1. Please identify all inventory that you have within your possession and cease use immediately.\n\n2. 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. Upon receipt of this record, Centurion Representative will contact you regarding retrieval of the product from your facility.\n\n3. Please forward this recall information to any facilities to who this product may have been further distributed, instructing them to cease use immediately.",
      "product_quantity": "200 kits",
      "distribution_pattern": "IL",
      "openfda": {
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        "device_name": "Dressing Change Tray",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5075",
        "device_class": "1"
      }
    }
  ]
}