{
  "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": "71851",
      "recalling_firm": "Lumenis",
      "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 - US including CA, PA, MA, FL, and NY, and Internationally to Italy,  Germany, Australia, China, Great Britian, United Kingdom, Taiwan, France, Peru, Mexico, Turkey, Spain, and Russia.",
      "recall_number": "Z-2770-2015",
      "product_description": "Lumenis VersaCut+ Tissue Morcellator GA-0007500    The Lumenis VersaCut / VersaCut+ Tissue Morcellator System is intended for use under direct or endoscopic visualization for the morcellation and removal of dissected tissue during pelviscopic, laparoscopic, percutaneous, and open surgical procedures whenever access to the surgical site is limited.",
      "product_quantity": "54 devices with 108 hand pieces",
      "reason_for_recall": "There is a probability the hand piece may operate inconsistently and unpredictably during the morcellation procedure resulting in damage to non-target tissue.",
      "recall_initiation_date": "20150730",
      "center_classification_date": "20150916",
      "termination_date": "20180525",
      "report_date": "20150923",
      "code_info": "GA-0007500 (VersaCut + System with Inverted H/P) and GA-0007600 (VersaCut + System with Regular H/P).  Only the hand pieces for the system (SA4769200 inverted HP, SA4768700 regular HP) are affected by this recall.",
      "more_code_info": ""
    }
  ]
}