{
  "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-2296-2021",
      "product_description": "DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system:  a) REF 3832572   b) REF 3842572  c) REF 3821572  d) REF 3833572  e) REF 3831572  f) REF 3810572  g) REF 3852572",
      "product_quantity": "203,680 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 3832572: Lot 11T80189  b) REF 3842572, Lot 11T80198  c) REF 3821572, Lot 11T80149  d) REF 3833572, Lot 11T80292  e) REF 3831572, Lot 12T80230  f) REF 3810572, Lot 12T80302  g) REF 3852572, Lot 12T80349"
    }
  ]
}