{
  "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-2295-2021",
      "product_description": "DELTAVEN Safety I.V. Catheter in Pur with closed system:  a) REF 3836272  b) REF 3814272  c) REF 3845272  d) REF 3856272",
      "product_quantity": "30,900 units",
      "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 3836272, Lot 11T80188  b) REF 3814272, Lot 11T80272  c) REF 3845272, Lot 12T80147  d) REF 3856272, Lot 12T80347"
    }
  ]
}