{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82350",
      "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": "Distributed to accounts in AL, CA, DC, FL, LA, MD, NE, TN, VA, and WA.",
      "recall_number": "Z-1120-2019",
      "product_description": "Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07",
      "product_quantity": "21220 total cases of 20",
      "reason_for_recall": "The firm has initiated a recall due to a confirmed complaint trend for  kinked tubing on the specified lots of the product.",
      "recall_initiation_date": "20190305",
      "center_classification_date": "20190410",
      "termination_date": "20200715",
      "report_date": "20190417",
      "code_info": "18105594  18105595  18105596  18105597"
    }
  ]
}