{
  "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-1648-2021",
      "product_description": "10G COAXIAL CANNULA WITH TUOHY CONNECTION, CODE INTVM-CC",
      "product_quantity": "40 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": "LOT:  20102495"
    }
  ]
}