{
  "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": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "The recall was initiated because Carefusion has confirmed that when the PAS 2000 drawers due to inaccessability of drawers caused by system down time or lock-up.",
      "address_2": "",
      "product_quantity": "2637",
      "code_info": "All Pyxis Anesthesia System Model 2000",
      "center_classification_date": "20130328",
      "distribution_pattern": "Worldwide Distribution - USA (Nationwide) including CANADA.",
      "state": "CA",
      "product_description": "Pyxis Anesthesia System Model 2000 (PAS 2000)      Product Usage:  The PAS 2000 is an anesthesia medication dispensing device that provides medications and inventory management for the anesthesiologist at the point of care within the operating room.",
      "report_date": "20130403",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion Corporation",
      "recall_number": "Z-1015-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "53991",
      "termination_date": "20130328",
      "more_code_info": "",
      "recall_initiation_date": "20091120",
      "postal_code": "92121",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}