{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Farnborough",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95642",
      "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": "U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.",
      "recall_number": "Z-0557-2025",
      "product_description": "Tempus LS-Manual Defibrillator  Model 00-3020    The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode",
      "product_quantity": "",
      "reason_for_recall": "Due to incorrect labels applied to devices during servicing.  Labels contain the incorrect product name and CAT number.",
      "recall_initiation_date": "20241028",
      "center_classification_date": "20241126",
      "report_date": "20241204",
      "code_info": "Model Number: 00-3020 UDI-DI code: 07613365002737 Serial Numbers: 7022.000367 7022.000387 7022.000392 7022.000462 7022.000463 7022.000464 7022.000559 7022.000591 7022.000595 7022.000711 7022.000781 7022.000786 7022.00108 7022.001175 7022.001201 7022.00129 7022.001556 7022.001582",
      "more_code_info": ""
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}