{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Farnborough",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91805",
      "recalling_firm": "Remote Diagnostic Technologies Ltd.",
      "address_1": "Farnborough Aerospace Centre",
      "address_2": "Aerospace Boulevard",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: U.S.(nationwide): AL, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, WI, WV, WY and O.U.S.(foreign): United Arab Emirates, Afghanistan, Austria, Australia, Belgium, Brunei Darussalam, Bolivia, Canada, Switzerland, Czechia, Germany, Denmark, Spain, France, United Kingdom, Hong Kong, Ireland, Israel, Iceland, Italy, Cayman Islands, Luxembourg, Malaysia, Netherlands, Norway, Portugal, Romania, Saudi Arabia, Sweden, Singapore, Slovenia, Thailand, Mayotte, and South Africa.",
      "recall_number": "Z-1321-2023",
      "product_description": "Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified personnel, for the attended or unattended monitoring of single or multiple vital signs in clinical and pre hospital care applications.    The affected power supplies are related to the following Tempus Pro Patient Monitoring units:    Model Numbers:  00-1004  00-1004-R  00-1007  00-1007-R  00-1024-R  00-1026-R  Model Numbers:  00-1004  00-1004-R  00-1007  00-1007-R  00-1024-R  00-1026-R",
      "product_quantity": "5,540 units",
      "reason_for_recall": "During internal testing, Regulatory Compliance issues were identified regarding the Monitor and Power Supplies for fluid ingress and basic safety issues.",
      "recall_initiation_date": "20230223",
      "center_classification_date": "20230331",
      "report_date": "20230412",
      "code_info": "Model Numbers: 00-1004 00-1004-R UDI-DI Codes: 05060472440020 05060472442901  00-1007 00-1007-R UDI-DI Codes: 05060472440013 05060472442901  00-1024-R UDI-DI Codes: 05060472441027 05060472442925  00-1026-R UDI-DI Codes: 05060472441058 05060472442932  Lot Codes - All products manufactured are affected.",
      "more_code_info": ""
    }
  ]
}