{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Newark",
      "address_1": "500 Gbc Dr Ms 514",
      "reason_for_recall": "Siemens Healthcare Diagnostics has confirmed an increase in the rate of \u001cAbnormal Assay\u001d errors and calibration failures with the Dimension Vista B2MIC Flex reagent cartridge: Dimension Vista System Flex reagent cartridge and urine stabilizer B2MIC. In the unlikely event that a patient result is generated, a suppressed result would be in conflict with the patient\u0019s clinical status and other markers of renal injury.",
      "address_2": "PO BOX 6101",
      "product_quantity": "1637 units.",
      "code_info": "Lot #: 15037MA - foreign  15175MA - foreign  15204MA- foreign  15246MA (Distributed in US)  15267MA - foreign",
      "center_classification_date": "20160301",
      "distribution_pattern": "Worldwide Distribution and US in the state of CA.",
      "state": "DE",
      "product_description": "Dimension Vista System  B2 Microglobulin Flex reagent cartridge and urine stabilizer       Catalog #K7024  SMN: 10445889\tLot #15246MA    Product Usage:  The B2MIC method is an in vitro diagnostic test for the quantitative measurement of B2-microglobulin in human serum, heparinized plasma, EDTA plasma and urine on the Dimension Vista System. Measurements of B2-microglobulin aid in the diagnosis of active rheumatoid arthritis and kidney disease.",
      "report_date": "20160309",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-1030-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73080",
      "termination_date": "20170113",
      "recall_initiation_date": "20151103",
      "postal_code": "19702-2466",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}