{
  "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": "Ongoing",
      "city": "Viadana",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88234",
      "recalling_firm": "Delta Med SpA",
      "address_1": "Via Guido Rossa 20",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of FL and MN.",
      "recall_number": "Z-2304-2021",
      "product_description": "NEO DELTA SELFSAFE PUR T, I.V. Catheter:",
      "product_quantity": "N/A",
      "reason_for_recall": "Problems related to the sterilization of the medical devices; possible missing sterility of the medical device",
      "recall_initiation_date": "20210621",
      "center_classification_date": "20210816",
      "report_date": "20210825",
      "code_info": "REF 3738522, Lot 00A2160813  REF 3738822, Lot 00A1160822"
    }
  ]
}