{
  "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": "Piscataway",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94839",
      "recalling_firm": "Horiba Instruments Incorporated",
      "address_1": "20 Knightsbridge Rd",
      "address_2": "N/A",
      "postal_code": "08854-3913",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and Worldwide Distribution",
      "recall_number": "Z-2166-2024",
      "product_description": "HORIBA custom configured fluorescence instrument, modular Fluorolog-QM",
      "product_quantity": "4 units",
      "reason_for_recall": "HORIBA custom configured fluorescence instrument has a laser safety defect.  This custom configuration of the modular Instrument removed the primary light source and the excitation monochromator. A plastic cap was installed to plug the optical port, where a more durable beam stop should have been used. The defect may allow the class 4 laser beam to burn (or transmit) through the plastic cap to exit the protective enclosure.",
      "recall_initiation_date": "20240328",
      "center_classification_date": "20240701",
      "report_date": "20240710",
      "code_info": "Modular Fluorolog-QM"
    }
  ]
}