{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70107",
      "recalling_firm": "BD Biosciences, Systems & Reagents",
      "address_1": "2350 Qume Dr",
      "address_2": "N/A",
      "postal_code": "95131-1812",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution.  US Nationwide including Puerto Rico, China, Brazil, Japan, Guatemala, India, New Zealand, Australia,  Canada, Thailand, Chile and Malaysia.",
      "recall_number": "Z-1000-2015",
      "product_description": "CD8 (Leu-2a) PE (In vitro diagnostic), Catalog number 340046.    Hematology: Single color direct immunofluorescence reagent for enumerating percentages of mature human suppressor/cytotoxic (CD8+) lymphocytes in erythrocyte-lysed whole blood or peripheral blood mononuclear cell suspensions.",
      "product_quantity": "165 units",
      "reason_for_recall": "One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected staining pattern and incorrect patient data.",
      "recall_initiation_date": "20141219",
      "center_classification_date": "20150120",
      "termination_date": "20160223",
      "report_date": "20150128",
      "code_info": "Lot number 4220622, Expiry 2016-04-30."
    }
  ]
}