{
  "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": "Sparks",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63949",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "BD Diagnostic Systems",
      "address_2": "7 Loveton Circle",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA including CT, FL, IL, KS, MD, MI, MO, NY, PA, RI, TX and WI.  Internationally to Canada, Europe and Japan.",
      "recall_number": "Z-0701-2013",
      "product_description": "Becton, Dickinson and Company,  BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.",
      "product_quantity": "86 Instruments",
      "reason_for_recall": "Clinical diagnostic instrument may exhibit minor defects, which could lead to erroneous test results.",
      "recall_initiation_date": "20120918",
      "center_classification_date": "20130122",
      "termination_date": "20130204",
      "report_date": "20130130",
      "code_info": "Serial Numbers:    MX0001 to MX0065   CM0001 to CM0105    NOTE:  Serial numbers are assigned sequentially.  The above ranges will include all sequential numbers in between the beginning and end points."
    }
  ]
}