{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Williamston",
      "address_1": "100 Centurion Way",
      "reason_for_recall": "Supplier initiated recall  of the GRIPPER Needles",
      "address_2": "",
      "product_quantity": "11260 kits",
      "code_info": "Lot Number      Expiration  2018121350 8/31/2020  2019020750 9/30/2020  2019031550 4/30/2021  2019041550 4/30/2021  2019061750 1/31/2021  2019062450 4/30/2021",
      "center_classification_date": "20191031",
      "distribution_pattern": "IL",
      "state": "MI",
      "product_description": "Kit, Port Access  Product Code: DYNDC1582A",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Centurion Medical Products Corporation",
      "recall_number": "Z-0255-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83542",
      "termination_date": "20200831",
      "more_code_info": "",
      "recall_initiation_date": "20190715",
      "postal_code": "48895-9086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}