{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "55350",
      "product_res_number": "Z-0555-2007",
      "event_date_initiated": "2007-08-13",
      "event_date_posted": "2007-09-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-28",
      "res_event_number": "39378",
      "product_code": "BRY",
      "product_description": "Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Diego, CA",
      "code_info": "All serial numbers of the Pyxis Anesthesia Station, Model 3500",
      "firm_fei_number": "3003879246",
      "recalling_firm": "Cardinal Health 303 Inc DBA Alaris Products",
      "address_1": "10221 Wateridge Cir",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121-2733",
      "additional_info_contact": "Stacy L. Lewis\n858-458-7830",
      "reason_for_recall": "System lock up; mini-drawers -under certain circumstances during use, are not accessable, delaying the user from accessing critical medications.",
      "root_cause_description": "Other",
      "action": "The field action consisted of phone calls and a mailing conducted to all customers for the Pyxis Anesthesia System 3500 beginning on 08/13/2007.  The customers will be notified by registered return receipt mail by Recall Notifications dated August 14, 2007. Separate letters will be sent to the Director of Pharmacy, Chief of Anesthesia, Director of Risk Management, and Director of Surgery at each facility.  Recommended actions will be provided as a short-term fix and a long-term fix of the software will be issued shortly.",
      "product_quantity": "369",
      "distribution_pattern": "Nationwide to Arizona, California, Colorado, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Louisiana, Massachusetts, Missouri, Mississippi, Montana, New Jersey, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Vermont, and Wyoming.",
      "openfda": {
        "registration_number": [
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        "fei_number": [
          "3011647251",
          "2024242",
          "1000115734",
          "3004574120",
          "3007880912",
          "3031700059",
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        ],
        "device_name": "Cabinet, Table And Tray, Anesthesia",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.6100",
        "device_class": "1",
        "k_number": [
          "K821307",
          "K871564",
          "K901474",
          "K921710",
          "K912346"
        ]
      }
    }
  ]
}