{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hayward",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67835",
      "recalling_firm": "Solta Medical, Inc.",
      "address_1": "25881 Industrial Blvd",
      "address_2": "N/A",
      "postal_code": "94545-2991",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution",
      "recall_number": "Z-1463-2014",
      "product_description": "FRAXEL DUAL 1550/1927 Laser System, (FRAXEL SR 1500 DUAL Laser System), for dermatological procedures.",
      "product_quantity": "1077 units",
      "reason_for_recall": "Obsolete versions of the Laser Treatment Settings card for the Fraxel DUAL 1550/1927 Laser system may have contained incorrect indication for use for treatment of Melasma.",
      "recall_initiation_date": "20140320",
      "center_classification_date": "20140416",
      "termination_date": "20150427",
      "report_date": "20140423",
      "code_info": "Model MC-SYS-SR1500-D, Revisions A and B."
    }
  ]
}