{
  "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,
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  "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": "240 kits",
      "code_info": "Lot Number      Expiration  2018110501 7/31/2021  2018121801 7/31/2021  2019013001 9/30/2021  2019032901 9/30/2021",
      "center_classification_date": "20191031",
      "distribution_pattern": "IL",
      "state": "MI",
      "product_description": "Maintenance Flush Kit/Blood Draw  Product Code: DT19335",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Centurion Medical Products Corporation",
      "recall_number": "Z-0254-2020",
      "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"
    }
  ]
}