{
  "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": "Wakefield",
      "address_1": "100 Quannapowitt Parkway",
      "reason_for_recall": "Notes associated with prescription are not printed to the prescription or to the patient chart.",
      "address_2": "Suite 405",
      "product_quantity": "35",
      "code_info": "Software Versions 5.2 and 5.3",
      "center_classification_date": "20130729",
      "distribution_pattern": "Nationwide Distribution, including the states of:  AK, AR, AZ, CA, CO, DC, DE, FL, GA, ID, IN, MA, MD, MO, NH, NJ, OH, OR, SC, TN, WA, and WV.",
      "state": "MA",
      "product_description": "Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3.  The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.",
      "report_date": "20130807",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Picis Inc.",
      "recall_number": "Z-1814-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65666",
      "termination_date": "20141219",
      "more_code_info": "",
      "recall_initiation_date": "20130621",
      "postal_code": "01880",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}