{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Grove City",
      "address_1": "3600 Gantz Rd",
      "reason_for_recall": "Analyzers were distributed with software which lacks a 510K",
      "address_2": "",
      "product_quantity": "8 units",
      "code_info": "Serial Numbers: 14646304, 14917201, 14886112, 14616503, 14856212, 14887601, 14886212 & 14917201",
      "center_classification_date": "20180925",
      "distribution_pattern": "US Nationwide Distribution in states of - CA, OK, VA 7 WI",
      "state": "OH",
      "product_description": "G8 Automated HPLC Analyzer - 723G8    Product Usage - In vitro diagnostic use for the quantitative measurement of % hemoglobin A1c in whole blood specimens. This test is to be used as an aid in the diagnosis of diabetes and as an aid in identifying patients who may be at risk for developing diabetes.",
      "report_date": "20181003",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tosoh Bioscience Inc",
      "recall_number": "Z-3244-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "80585",
      "termination_date": "20200708",
      "more_code_info": "",
      "recall_initiation_date": "20180713",
      "postal_code": "43123-1895",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}