{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Republic",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85591",
      "recalling_firm": "ROi CPS LLC",
      "address_1": "3000 E Sawyer Rd",
      "address_2": "N/A",
      "postal_code": "65738-2758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution in the states of MO, AR and OK.",
      "recall_number": "Z-2265-2020",
      "product_description": "Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.",
      "product_quantity": "40 Kits.",
      "reason_for_recall": "Custom procedure kits contains affected lots of PosiFlush Syringe, a product recalled by BD.",
      "recall_initiation_date": "20200420",
      "center_classification_date": "20200605",
      "termination_date": "20200821",
      "report_date": "20200617",
      "code_info": "Lot no. 68336DRW. Item number: 830034. UDI: (01) 10326053106634 (17) 210131 (10) 68336DRW."
    }
  ]
}