{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Tarrytown",
      "address_1": "511 Benedict Ave",
      "reason_for_recall": "There is a potential for falsely depressed creatinine results for patients on phenindione therapy when using the enzymatic methodology. Interference has not been observed with the creatinine Jaffe methodology.",
      "address_2": "",
      "product_quantity": "1,015 units",
      "code_info": "UDI Number: 00630414526690  Lots: All lots",
      "center_classification_date": "20200214",
      "distribution_pattern": "US Nationwide",
      "state": "NY",
      "product_description": "ADVIA Chemistry Enzymatic Creatinine (ECRE_2) reagent, SMN 10335869",
      "report_date": "20200226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "recall_number": "Z-1230-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84612",
      "termination_date": "20200625",
      "more_code_info": "",
      "recall_initiation_date": "20191218",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}