{
  "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": "Tosoh Bioscience has become aware of a potential issue with the pickup arm and pickup arm motor on the AIA-900 Analyzer. If the pickup arm or pickup arm motor malfunctions, the analyzer will cease to function and result in an inability to test patient samples. This may cause a delay in testing and reporting patient results. Tosoh has received fifty-one (51) complaints related to this issue with no serious injuries reported.",
      "address_2": "",
      "product_quantity": "393",
      "code_info": "All units are affected",
      "center_classification_date": "20181114",
      "distribution_pattern": "Distributed nationwide. Foreign distribution to Canada and Latin America.",
      "state": "OH",
      "product_description": "AIA-900 Analyzer, Product code 022930, 022930R",
      "report_date": "20181121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tosoh Bioscience Inc",
      "recall_number": "Z-0469-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81187",
      "termination_date": "20201110",
      "more_code_info": "",
      "recall_initiation_date": "20181005",
      "postal_code": "43123-1895",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}