{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Yokne'Am Ilit",
      "state": "N/A",
      "country": "Israel",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97279",
      "recalling_firm": "LUMENIS, LTD.",
      "address_1": "Yokneam Ind. Park",
      "address_2": "6, Ha-Kidma",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic: PA, WI; International: Germany, India;",
      "recall_number": "Z-2344-2025",
      "product_description": "OtoLase Starter Kit;  UPN: AC-2003748.  Indicated for a  variety of surgical uses including ablation, coagulation, incision, excision, and vaporization of soft tissue.",
      "product_quantity": "13 units",
      "reason_for_recall": "The potential for unsterilized product within finished product labeled as sterile.",
      "recall_initiation_date": "20250722",
      "center_classification_date": "20250821",
      "report_date": "20250827",
      "code_info": "UPN: AC-2003748; UDI-DI: 07290109142807; Batch Numbers: 32644549 and 32769567; Expiration Date: 22Aug2025;"
    }
  ]
}