{
  "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": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92251",
      "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": "US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.",
      "recall_number": "Z-1825-2023",
      "product_description": "Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020",
      "product_quantity": "1147",
      "reason_for_recall": "Defibrillator/pacemaker module (DPM) may encounter a problem causing communication from the Mainboard  to the DPM to fail, leading to no or ineffective pacing with displayed error message \"HW failure DPM\".",
      "recall_initiation_date": "20230508",
      "center_classification_date": "20230612",
      "report_date": "20230621",
      "code_info": "UDI-DI: 07613365002737. Serial numbers prior to 7022.001634"
    }
  ]
}