{
  "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": "Yokneam",
      "state": "",
      "country": "Israel",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75384",
      "recalling_firm": "Lumenis Limited",
      "address_1": "13 Hayetzira St.,Yokneam Ind. Park",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- USA, Italy, Russian Fed., Australia, United Arab Emirates, Spain, United Kingdom, India, Kuwait, and Belarus.",
      "recall_number": "Z-0301-2017",
      "product_description": "FemTouch delivery system includes the FemTouch Kit (AC-1007415) and FemTouch\" Tip (SPSA-20002590)    Provide fractional treatments in gynecology.",
      "product_quantity": "69 units",
      "reason_for_recall": "The cleaning instructions provided in FemTouch Operator\u0019's Manual might be ineffective for a fully assembled device and may lead to a potential for cross-contamination.",
      "recall_initiation_date": "20160925",
      "center_classification_date": "20161023",
      "termination_date": "20170411",
      "report_date": "20161102",
      "code_info": "All serial numbers",
      "more_code_info": ""
    }
  ]
}