{
  "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-2298-2021",
      "product_description": "DELTAVEN Y, Safety I.V. Catheter in Pur with closed system  a) REF 3832072  b) REF 3810072  c) REF 3842072  d) REF 3852072",
      "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": "a) REF 3832072, Lot 11T80190  b) REF 3810072, Lot 11T80303  c) REF 3842072, Lot 12T80342  d) REF 3852072, Lot 12T80348"
    }
  ]
}