{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Suzhou",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93146",
      "recalling_firm": "Carl Zeiss Suzhou Co., Ltd.",
      "address_1": "Modern Industrial Square 3b",
      "address_2": "No. 333 Xingpu Road; Kunshan",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MD, TX, CA, GA, LA.",
      "recall_number": "Z-0183-2024",
      "product_description": "OPMI LUMERA 300, REF 6137",
      "product_quantity": "8",
      "reason_for_recall": "Surgical microscope for use in ophthalmology may be missing a screw from the suspension arm, which may cause the suspended components to fall from the suspension arm, which may injure any person under the suspended components.",
      "recall_initiation_date": "20230818",
      "center_classification_date": "20231026",
      "report_date": "20231101",
      "code_info": "UDI-DI/Serial Numbers: 06909262061375/6137104455, 6137104627, 6137104623, 6137104678, 6137104233, 6137104620, 6137104480, 6137104613"
    }
  ]
}