{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Grove City",
      "address_1": "3600 Gantz Rd",
      "reason_for_recall": "",
      "address_2": "",
      "product_quantity": "992 units",
      "code_info": "all lots",
      "center_classification_date": "20181222",
      "distribution_pattern": "US Nationwide",
      "state": "OH",
      "product_description": "ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of homocysteine in human serum, heparinized plasma or EDT A plasma on TOSOH AIA System Analyzers. Homocysteine measurements are used in the diagnosis and treatment of hyperhomocysteinemia or homocysteinuria.",
      "report_date": "20190102",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tosoh Bioscience Inc",
      "recall_number": "Z-0675-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81597",
      "termination_date": "20210114",
      "more_code_info": "",
      "recall_initiation_date": "20181130",
      "postal_code": "43123-1895",
      "voluntary_mandated": "Voluntary: Firm initiated",
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