{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Medolla",
      "state": "",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87926",
      "recalling_firm": "RanD S.r.l.",
      "address_1": "Strada Statale 62",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  FL, IL, TN, WI",
      "recall_number": "Z-2048-2021",
      "product_description": "Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120",
      "product_quantity": "72",
      "reason_for_recall": "The sterilization contractor informed the company of a quality issue possibly affecting the sterilization process of a certain number of products.  It was determined that some lots may not be sterile.",
      "recall_initiation_date": "20210430",
      "center_classification_date": "20210709",
      "termination_date": "20240205",
      "report_date": "20210721",
      "code_info": "Lot Numbers: F180266  F180315  F190169",
      "more_code_info": ""
    }
  ]
}