{
  "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": "Roseville",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75048",
      "recalling_firm": "New Star Lasers, Inc.",
      "address_1": "9085 Foothills Blvd",
      "address_2": "N/A",
      "postal_code": "95747-7130",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution only.",
      "recall_number": "Z-2916-2016",
      "product_description": "ReNew (a.k.a. Trio)    Dermatology:  for use in dermatology for incision, excision, ablation and vaporization with hemostasis of soft tissue;  for use in the treatment of fine lines and wrinkles;  for treatment of back acne and atrophic acne scars;  for treatment of reflux of the great and small saphenous veins associated with varicose veins and varicosities, and; for laser assisted lipolysis",
      "product_quantity": "5 systems",
      "reason_for_recall": "FDA inspection found that customers who had received devices with promotional material  with outside use indications were not notified when labeling was revised to remove these indications.",
      "recall_initiation_date": "20160919",
      "center_classification_date": "20160930",
      "termination_date": "20161213",
      "report_date": "20161012",
      "code_info": "Serial numbers:  ABKK03  ABKK04  ABKM02  ABSG01  ABUP01."
    }
  ]
}