{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "EDEN PRAIRIE",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77170",
      "recalling_firm": "Laserex Systems Inc.",
      "address_1": "7138 SHADY OAK RD",
      "address_2": "N/A",
      "postal_code": "55344-3517",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution",
      "recall_number": "Z-2172-2017",
      "product_description": "Ellex Tango Reflex  with slit lamp Laser Ophthalmic    In the SLT mode, the device is intended to be used for selective laser trabeculoplasty (ST) operations (laser trabeculoplasty for primary open angle glaucoma). In the VAG mode it is intended to be used to perform procedures requiring the rupture of tissue in the eye for Iridotomy and Iridectomy, Posterior capsulotomy and Posterior membranectomy.",
      "product_quantity": "83",
      "reason_for_recall": "It was discovered the unit produced a laser emission without pressing the fire button when the slit-lamp  was driven to its lowest  position prior to use on any patient.",
      "recall_initiation_date": "20170404",
      "center_classification_date": "20170606",
      "termination_date": "20170731",
      "report_date": "20170614",
      "code_info": "Serial No: TR 0010,  TR 0095"
    }
  ]
}