{
  "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": "San Giovanni In Persiceto",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88543",
      "recalling_firm": "ADRIA SRL",
      "address_1": "Via Modena 46",
      "address_2": "Societa Unipersonale",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states: NJ and NY.",
      "recall_number": "Z-0144-2022",
      "product_description": "Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715",
      "product_quantity": "N/A",
      "reason_for_recall": "The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.",
      "recall_initiation_date": "20210517",
      "center_classification_date": "20211019",
      "termination_date": "20231106",
      "report_date": "20211027",
      "code_info": "Lot Number: AD0316/20"
    }
  ]
}