{
  "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": "87158",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution US nationwide and Canada",
      "recall_number": "Z-1109-2021",
      "product_description": "BD Hypodermic Syringe 10 ml, eccentric tip.  Catalog (Ref No.) 305482",
      "product_quantity": "155,200 needles",
      "reason_for_recall": "The product packaging for the 10 ml eccentric tip syringe may exhibit open seals.  An open seal impacts package integrity and potentially compromises sterility of the syringe.",
      "recall_initiation_date": "20201223",
      "center_classification_date": "20210212",
      "termination_date": "20221121",
      "report_date": "20210224",
      "code_info": "Catalog (Ref No.) 305482  100/package    UDI 00382903054824    Lot # 8142303    exp date 31-May-2023"
    }
  ]
}