{
  "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-1839-2021",
      "product_description": "NICO Myriad-LX Illumination Pack:  REF: NN-1000 Mvriad-LX Illumination Pack. 11ga  REF: NN-1001 Mvriad-LX Illumination Pack. l3ga    Intended to perform resection and removal of soft tissues and fluids under direct visualization accessories to the NICO Myriad System.",
      "product_quantity": "439 packs",
      "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": "Lot Numbers:  37KII300  37KI1301  37LI0320  37LI0322  37AJ1438  37AJ1439  37BJ0513  37BJ0516  37CJ0203  37CJ0204  37GJ1603  37GJ1607  37110208  37IJ0209"
    }
  ]
}