{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Newark",
      "state": "DE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90872",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "500 Gbc Dr",
      "address_2": "N/A",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Foreign: Canada",
      "recall_number": "Z-0089-2023",
      "product_description": "Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent cartridge, IVD  Siemens Material Number (SMN): 10464340\t  Catalog Number: K3048A",
      "product_quantity": "1592 units",
      "reason_for_recall": "Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for Erroneous Result. If an HDLC QC or patient result is obtained without an  Abnormal Reaction  [E145]: flag, a falsely depressed or elevated result ranging from -90% to 133% may be observed.",
      "recall_initiation_date": "20220824",
      "center_classification_date": "20221014",
      "report_date": "20221026",
      "code_info": "UDI-DI : 0084276802043821250BA2022090710464340840 Lot Number: 21250BA Exp. Date: 2022-09-07",
      "more_code_info": ""
    }
  ]
}