{
  "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": "In vitro diagnostic test kit may exhibit invalid internal negative control results.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "177 kits",
      "code_info": "Cat #446257: Lot 3035126  Exp 12/04/13  Cat #446252: Lot 3065261  Exp 08/31/13",
      "center_classification_date": "20130726",
      "distribution_pattern": "Nationwide Distribution",
      "state": "MD",
      "product_description": "BD Affirm VPIII Microbial Identification Tests, packaged in kits, 120 test\\kit, Catalog # 446257 and 24 test\\kit, Catalog # 446252; kits are labeled in part ***Becton, Dickinson and Company, 7 Loveton Circle Sparks, MD 21152 USA, 800-638-8663, www.bd.com/ds***    The Affirm VPIII Microbial Identification Test is a DNA probe test intended for use in the detection and identification of Candida species,",
      "report_date": "20130807",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-1812-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65619",
      "termination_date": "20130928",
      "more_code_info": "",
      "recall_initiation_date": "20130613",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}