{
  "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 Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89185",
      "recalling_firm": "Velano Vascular",
      "address_1": "221 Pine St # 200",
      "address_2": "",
      "postal_code": "94104-2705",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CT, CO, UT, PA, IL, WA, CA, NJ, MI, FL, NC.",
      "recall_number": "Z-0527-2022",
      "product_description": "PIVO Blood Collection Device 20G, REF: 202-0005",
      "product_quantity": "123,700",
      "reason_for_recall": "Incomplete sealing of blood collection device unit packages may produce a breach in the sterile barrier enclosing the product. This could lead to microbial contamination of the device prior to use. The health effects range from no clinical effect up to bloodstream infection.",
      "recall_initiation_date": "20211110",
      "center_classification_date": "20220125",
      "termination_date": "20230731",
      "report_date": "20220202",
      "code_info": "UDI: 00850984007027. Lots: 070621-02, 062221-01, 061021-02, 052721-03, 051421-02",
      "more_code_info": ""
    }
  ]
}