{
  "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": [
    {
      "country": "United States",
      "city": "Culver City",
      "address_1": "8550 Higuera St",
      "reason_for_recall": "The firm is initiating this recall of  the SL3 Soft Tissue Laser equipped with a fiber optic Unifiber system which contains a fragile glass filament because the fiber broke near the hand piece.",
      "address_2": "",
      "product_quantity": "150 units",
      "code_info": "Model LR2002",
      "center_classification_date": "20130429",
      "distribution_pattern": "Nationwide Distribution including AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MO, MT NH, NJ, NM, NV, NY, OH, PA, SD, TX, UT, VA, and WA.",
      "state": "CA",
      "product_description": "SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA 90232.    The SL3 is a soft-tissue diode laser intended to be used for dental procedures",
      "report_date": "20130508",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Discus Dental LLC",
      "recall_number": "Z-1186-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64621",
      "termination_date": "20130429",
      "more_code_info": "",
      "recall_initiation_date": "20110721",
      "postal_code": "90232-2522",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}