{
  "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": {
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      "status": "Terminated",
      "city": "Basingstoke",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89595",
      "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": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of IL and KS.",
      "recall_number": "Z-0861-2022",
      "product_description": "Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693",
      "product_quantity": "2",
      "reason_for_recall": "Distribution of Defibrillators that are not approved  or cleared for distribution US Market.",
      "recall_initiation_date": "20220128",
      "center_classification_date": "20220404",
      "termination_date": "20240725",
      "report_date": "20220413",
      "code_info": "Device Serial Numbers 7021.002073 and 7021.002074",
      "more_code_info": ""
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}