{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Tarrytown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92800",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "511 Benedict Ave",
      "address_2": "N/A",
      "postal_code": "10591-5005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide - Worldwide Distribution Foreign: Taiwan Uruguay Vietnam",
      "recall_number": "Z-2471-2023",
      "product_description": "Atellica CH Total Bilirubin_2 -In vitro diagnostic use in the  quantitative determination of total bilirubin in human serum and plasma (lithium heparin) of adults and neonates   Test Code: TBil_2  Siemens Material Number (SMN): 11097531",
      "product_quantity": "50148 units",
      "reason_for_recall": "Potential for reagent carryover on the Atellica CH 930 resulting in a positive bias that could impact quality control (QC), patient samples, and calibrator results with  from Atellica¿ CH Total Bilirubin_2 (TBil_2), Atellica¿CH LDL Cholesterol (LDLC), Atellica¿ CH Gamma-Glutamyl Transferase (GGT) and Atellica¿CH HDL Cholesterol (HDLC)",
      "recall_initiation_date": "20230710",
      "center_classification_date": "20230828",
      "report_date": "20230906",
      "code_info": "Unique Device Identification (UDI): 00630414595818 All Lot Numbers"
    }
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}