{
  "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": "San Jose",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70811",
      "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": "US Distribution in states of: MO, GA, AZ, NE, TX, VA",
      "recall_number": "Z-1375-2015",
      "product_description": "CD123 (9F5) PE    Catalog number 649453    Analyte Specific Reagent",
      "product_quantity": "9",
      "reason_for_recall": "One lot of BD CD123 PE (ASR) has been determined to contain a low amount of CD4 antibody  and may result in an unexpected staining pattern.",
      "recall_initiation_date": "20150323",
      "center_classification_date": "20150402",
      "termination_date": "20160226",
      "report_date": "20150408",
      "code_info": "Lot 5008762, Exp 11/30/16."
    }
  ]
}