{
  "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": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82273",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "address_2": "N/A",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of AR, NH, NC",
      "recall_number": "Z-1210-2019",
      "product_description": "SmartSite Syringe Administration Set-Product Package Size 50,   Catalog Number: 10798696",
      "product_quantity": "2900 Sets",
      "reason_for_recall": "Leaking of the Smartsite Syringe Administration Set.  May result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to infusates.",
      "recall_initiation_date": "20190228",
      "center_classification_date": "20190626",
      "termination_date": "20200730",
      "report_date": "20190703",
      "code_info": "Lot Number: 18046218  Exp. Date: 04/18/2021  UDI: 50885403234352"
    }
  ]
}