{
  "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": "2026-04-01",
    "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": "96053",
      "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": "Worldwide",
      "recall_number": "Z-0976-2025",
      "product_description": "BD Pyxis Med 4000 Auxiliary (AUX), REF 314",
      "product_quantity": "5 units",
      "reason_for_recall": "Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified:    Situation 1: Door Latch Failure,   Situation 2: Cable Ribbon Damage,   Situation 3: Magnet Falling Out,",
      "recall_initiation_date": "20230214",
      "center_classification_date": "20250117",
      "report_date": "20250129",
      "code_info": "UDI/DI 10885403512650, Serial Numbers:  16140589, 16194078, 16194079, 16194081, 16079165.",
      "more_code_info": ""
    }
  ]
}