{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "East Lansing",
      "address_1": "16429 Upton Rd",
      "reason_for_recall": "Failure to comply with the laser class limitation listed in the performance standard for Specific Use Laser products.",
      "address_2": "Suite #1",
      "product_quantity": "3",
      "code_info": "Surveying Leveling and Alignment (SLA) laser products",
      "center_classification_date": "20171208",
      "distribution_pattern": "US Distribution",
      "state": "MI",
      "product_description": "United Nuclear Scientific High Power Handheld Lasers.     Laser products",
      "report_date": "20171220",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "United Nuclear Scientific Supplies, LLC",
      "recall_number": "Z-0051-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78389",
      "termination_date": "20201027",
      "recall_initiation_date": "20160825",
      "postal_code": "48823-9327",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
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}