{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96002",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of NY, NC, LA.",
      "recall_number": "Z-0906-2025",
      "product_description": "BD Pyxis MedStation  ES (Med ES Main), REF: 323; and BD Pyxis MedStation  ES (Med ES Main Tower), REF: 352",
      "product_quantity": "622",
      "reason_for_recall": "Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display \"Server connection failed,\" not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.",
      "recall_initiation_date": "20230405",
      "center_classification_date": "20250114",
      "report_date": "20250122",
      "code_info": "Software v1.7.3. REF/UDI-DI: 323/10885403512667, 352/10885403512674",
      "more_code_info": ""
    }
  ]
}