{
  "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": [
    {
      "country": "United States",
      "city": "Sparks",
      "address_1": "BD Diagnostic Systems",
      "reason_for_recall": "PrepStain system rack setting was incorrectly entered on one PrepStain system during a routine preventive maintenance visit by a BD Field Service Representative.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "890 instruments",
      "code_info": "Catalog Numbers - 799-13000-00 and 799-13000-00R",
      "center_classification_date": "20130828",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and  Puerto Rico and the country of Canada.",
      "state": "MD",
      "product_description": "PrepStain Tecan US-I.    For use in the screening and detection of cervical cancer.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-2111-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65779",
      "termination_date": "20140501",
      "more_code_info": "",
      "recall_initiation_date": "20130708",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}