{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Grove City",
      "address_1": "3600 Gantz Rd",
      "reason_for_recall": "This recall has been initiated due to a potential malfunction of the photo interrupter (Pl). The potential  malfunction has been attributed to aging and premature deterioration of the Pl collector current.",
      "address_2": "",
      "product_quantity": "565 total devices U.S.",
      "code_info": "AIA-900 19tray Sorter with S/N 10000109 to S/N 80136909.  AIA-900 9tray Sorter with S/N 10000109 to S/N 10707402.",
      "center_classification_date": "20180130",
      "distribution_pattern": "Worldwide Distribution - U.S. Nationwide - Latin America",
      "state": "OH",
      "product_description": "Tosoh¿Sorter 9tray, Product Code 022931and Tosoh¿Sorter 19tray, Product Code 022932.    Product Usage:  The AIA-900 9tray Sorter and AIA-900 19tray Sorter supports the automation of the AIA-900 systems.",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tosoh Bioscience Inc",
      "recall_number": "Z-0492-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "78776",
      "termination_date": "20191231",
      "more_code_info": "",
      "recall_initiation_date": "20170611",
      "postal_code": "43123-1895",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}