{
  "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": "Haifahaifa",
      "state": "",
      "country": "Israel",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79186",
      "recalling_firm": "Argo Medical Technologies Ltd",
      "address_1": "Matambuilding 30p.O.Box 15054",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and foreign.",
      "recall_number": "Z-0944-2018",
      "product_description": "ReWalk Personal 6.0. Catalog number: 50-20-0004.",
      "product_quantity": "127",
      "reason_for_recall": "Firm received complaints for ReWalk Personal 6.0 of an injury to tibia and fibula.",
      "recall_initiation_date": "20170814",
      "center_classification_date": "20180309",
      "termination_date": "20191112",
      "report_date": "20180321",
      "code_info": "Date range of Distribution: 09/01/2015 to 09/06/2017.",
      "more_code_info": ""
    }
  ]
}