{
  "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": "An antibiotic susceptibility test kit may produce false intermediate or false resistant results with clinically significant bacteria.",
      "address_2": "7 Loveton Circle",
      "product_quantity": "12,250 tests",
      "code_info": "Lot number 2053373",
      "center_classification_date": "20121219",
      "distribution_pattern": "Nationwide distribution: USA including states of: AR, CA, KY, OK, RI, WI, and WY.",
      "state": "MD",
      "product_description": "BD Phoenix PMIC-108 Panels, Catalog number 448418, labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, USA.    The BD Phoenix\" Automated Microbiology system is intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria.",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Co.",
      "recall_number": "Z-0570-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63737",
      "termination_date": "20130109",
      "more_code_info": "",
      "recall_initiation_date": "20121106",
      "postal_code": "21152-0999",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}