{
  "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": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87882",
      "recalling_firm": "Nico Corp.",
      "address_1": "250 E 96th St Ste 125",
      "address_2": "N/A",
      "postal_code": "46240-3872",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1840-2021",
      "product_description": "Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection  Part Number NN-7013    The Myriad-LX light source is a high-intensity 300W Xenon illuminator with a touch screen and digital dimming controls. The source is fitted with a proprietary connector to ensure usage is reserved for the Myriad-LX Illumination Fiber.",
      "product_quantity": "80 units",
      "reason_for_recall": "(1) Updated IFU for the LX Illumination Packs:   Warning - Avoid contact between the distal opening of the delivery sleeve and tissue/debris within the surgical.field to prevent complete occlusion. Some surgical approaches (e.g., endonasal) may increase this potential. {f unintended reduction in light output occurs and/or occlusion of the sleeve is suspected, both the delivery sleeve and the fiber should be replaced    (2) Removal for the LX Light Source potential for the distal tip of the sleeve/fiber assembly  potential to burn healthy tissue resulting in minor to moderate injury to the patient or end user.",
      "recall_initiation_date": "20210430",
      "center_classification_date": "20210609",
      "termination_date": "20240205",
      "report_date": "20210616",
      "code_info": "Serial Numbers  350-00194D  350-00355D  350-00356D  350-00357D  350-00376D through 350-00444D  350-00451D through 350-00460D  350-00463D through 350-00467D  350-004710 through 350-00475D"
    }
  ]
}