{
  "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": "Mirandola",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87696",
      "recalling_firm": "BIOPSYBELL S.R.L.",
      "address_1": "Via Aldo Manuzio N. 24",
      "address_2": "Via A.Manuzio n.24",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states MS and KY.",
      "recall_number": "Z-1636-2021",
      "product_description": "EASYNJECT, Device for cement infusion in the vertebroplasty procedure, REF KVTGUN-DS",
      "product_quantity": "5 units",
      "reason_for_recall": "Products labeled as sterile were distributed, but may not have been sterilized.",
      "recall_initiation_date": "20210322",
      "center_classification_date": "20210519",
      "termination_date": "20260217",
      "report_date": "20210526",
      "code_info": "BATCH:2003721"
    }
  ]
}