{
  "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": "Mawson Lakes",
      "state": "N/A",
      "country": "Australia",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92532",
      "recalling_firm": "Ellex Medical Pty Ltd.",
      "address_1": "3-4 Second Ave",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US nationwide/ Worldwide Distribution",
      "recall_number": "Z-1971-2023",
      "product_description": "Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532  Spare, Optics Bench V2, L2G/LP6G",
      "product_quantity": "57 systems in total (6 units shipped to United States)",
      "reason_for_recall": "When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a scattered laser beam inside the laser cavity system may unintentionally exit through the Slit Lamp output port (SDS) and get emitted from the Objective Lens when the laser is fired.",
      "recall_initiation_date": "20230316",
      "center_classification_date": "20230627",
      "report_date": "20230705",
      "code_info": "Serial Nos., UDI IPY0374, (01) 0 9342395 00012 0 ISRY0242, (01) 0 9342395 00015 1 ISG0370, (01) 0 9342395 00024 3 IPG0539, (01) 0 9342395 00009 0 BG1190",
      "more_code_info": ""
    }
  ]
}