{
  "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": "2026-04-08",
    "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": "82138",
      "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": "The products were distributed to the following US states:  FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, and WI.    The products were distributed to the following foreign countries:  Suriname.",
      "recall_number": "Z-2008-2019",
      "product_description": "3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061",
      "product_quantity": "428,800",
      "reason_for_recall": "The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.",
      "recall_initiation_date": "20190201",
      "center_classification_date": "20190722",
      "termination_date": "20200611",
      "report_date": "20190731",
      "code_info": "Lot Number 8307694"
    }
  ]
}