{
  "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": "Basingstoke",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88051",
      "recalling_firm": "Remote Diagnostic Technologies Ltd.",
      "address_1": "PAVILION C2, ASHWOOD PARK",
      "address_2": "ASHWOOD WAY",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of FL, TX, PA, MN, UT, MT, CA, WI, VA, NY, TN, KS, MD and the countries of Australia, Austria, Czech Republic, France, Germany, Hong Kong, Israel, Italy, Netherlands, Thailand, Abu Dhabi, UK.",
      "recall_number": "Z-1997-2021",
      "product_description": "Tempus Pro - Patient  physiological monitor, arrhythmia detector and alarm.  Part No. - 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. Product Usage: intended to be used as a stand-alone monitor or as a telemedicine system (transmitting patient data to other medical professionals located elsewhere).",
      "product_quantity": "510 systems",
      "reason_for_recall": "The Tempus Pro (Trizeps 7 only) when used in combination with a specified laryngoscope device can cause two error types when subsequently unplugged.",
      "recall_initiation_date": "20210525",
      "center_classification_date": "20210701",
      "report_date": "20210707",
      "code_info": "Software version number: v07.00,  v07.01, v07.18, v07.20, v07.22, v07.24.     UDI No.                   12NC No.  05060472440020 989706002081  05060472440013 989706000001  05060472441027 989706000051  05060472441058    989706000101"
    }
  ]
}