{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "81511",
      "product_res_number": "Z-0365-2010",
      "event_date_initiated": "2009-04-08",
      "event_date_posted": "2009-11-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-12-22",
      "res_event_number": "51876",
      "product_code": "NSX",
      "product_description": "PICIS, CareSuite Family- OR Manager (4235), Preop Manager (4250), Anesthesia Manager (4220), PACU Manager (4245) & Critical Care Manager (1110), patient information systems.",
      "code_info": "Software version 7.2.2",
      "firm_fei_number": "3005244943",
      "recalling_firm": "Picis Inc.",
      "address_1": "100 Quannapowitt Parkway",
      "address_2": "Suite 405",
      "city": "Wakefield",
      "state": "MA",
      "postal_code": "01880",
      "additional_info_contact": "Same as Above\n781-557-3000",
      "reason_for_recall": "Demographic data, most notably allergy and precaution data, can be overwritten with incomplete data or blanks by the interface between non-Picis clinical systems (your \"HIS\" or \"CIS\") and certain Picis applications, if that interface is not configured properly.",
      "root_cause_description": "Software design",
      "action": "On April 8th 2009, Picis initiated a customer notification letter to the installed base of potentially affected users, explaining the potential source of patient data conflict and to provide support in choosing the appropriate configuration option and implementation. The notification letters included with this report package contain additional details regarding configuration options.",
      "product_quantity": "325",
      "distribution_pattern": "Worldwide distribution:  USA, Australia, Austria, Belgium, Denmark, Finland, France, Germany, Italy, Malaysia, Netherlands, Norway, Portugal, Singapore, Spain, Sweden, and United Kingdom",
      "openfda": {
        "registration_number": [
          "2024500",
          "3031158",
          "9611109",
          "1528142",
          "9611031",
          "3003587684",
          "3003971136"
        ],
        "fei_number": [
          "2024500",
          "3002807019",
          "1000122772",
          "3000215024",
          "3002808267",
          "3003587684",
          "3003971136"
        ]
      }
    }
  ]
}