{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tonsley",
      "state": "",
      "country": "Australia",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95603",
      "recalling_firm": "Micro-X Ltd.",
      "address_1": "Unit 14 6 Mab Eastern Promenade",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide and US Nationwide Distribution: NJ, PR, CA",
      "recall_number": "Z-0664-2025",
      "product_description": "MICRO-X Rover Mobile X-ray System, # MXU-RV35",
      "product_quantity": "5",
      "reason_for_recall": "Shots were terminated by the mAs integrator; however, the 4 ms exposure time did not allow enough tolerance to achieve diagnostic exposures due to variations in hardware and how different timers are started.",
      "recall_initiation_date": "20230531",
      "center_classification_date": "20241212",
      "report_date": "20241218",
      "code_info": "UDI-DI: 9357123000037. Serial Numbers: 00334, 00348, 00349, 00351, 00361.¿",
      "more_code_info": ""
    }
  ]
}