{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Thornwood",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84163",
      "recalling_firm": "Zeiss, Carl Inc",
      "address_1": "1 Zeiss Dr",
      "address_2": "N/A",
      "postal_code": "10594-1939",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide",
      "recall_number": "Z-1629-2020",
      "product_description": "Component for Laser Scanning Microscopes (LSM 700, LSM 800 and LSM 900)",
      "product_quantity": "US: 600; Global: 1600",
      "reason_for_recall": "When the user tilts the transmitted light arm of the microscope to the end of its axis range, laser safety can be bypassed and result in emission of class lIlb laser radiation. This issue arises when a ZEISS inverted stage stand (Axio Observer or Axio Vert) is used in as a component of the LSM 700, 800 and 900 system",
      "recall_initiation_date": "20191002",
      "center_classification_date": "20200406",
      "termination_date": "20240725",
      "report_date": "20200415",
      "code_info": "(LSM 700, LSM 800 and LSM 900)"
    }
  ]
}