{
  "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  2018092801 12/31/2019  2018121401 5/31/2020  2019022601 6/30/2020  2019032901 6/30/2020",
      "center_classification_date": "20191031",
      "distribution_pattern": "IL",
      "state": "MI",
      "product_description": "Port full Access Tray  Product Code: DT19330",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Centurion Medical Products Corporation",
      "recall_number": "Z-0253-2020",
      "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"
    }
  ]
}