{
  "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": "2026-04-22",
    "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": "66031",
      "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": "Distributed in the states of CT, KY, IL, NY, PA, TX, and VA and the country of Canada.",
      "recall_number": "Z-2192-2013",
      "product_description": "BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company,  Franklin Lakes, NJ 07417 USA Made in USA.    Used to perform heel sticks for the purpose of collecting skin puncture blood.",
      "product_quantity": "US - 39,800 units ; Canada - 18,400 units",
      "reason_for_recall": "The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.",
      "recall_initiation_date": "20130710",
      "center_classification_date": "20130911",
      "termination_date": "20140319",
      "report_date": "20130918",
      "code_info": "REF # 368101      Lot #3116007    Class I Exempt    Device listing Number E158602",
      "more_code_info": ""
    }
  ]
}