{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "160399",
      "product_res_number": "Z-0492-2018",
      "event_date_initiated": "2017-06-11",
      "event_date_created": "2018-01-31",
      "recall_status": "Terminated",
      "event_date_terminated": "2019-12-31",
      "res_event_number": "78776",
      "product_code": "KHO",
      "product_description": "TosohSorter 9tray, Product Code 022931and TosohSorter 19tray, Product Code 022932.\n\nProduct Usage:\nThe AIA-900 9tray Sorter and AIA-900 19tray Sorter supports the automation of the AIA-900 systems.",
      "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.",
      "firm_fei_number": "3005529799",
      "recalling_firm": "Tosoh Bioscience Inc",
      "address_1": "3600 Gantz Rd",
      "city": "Grove City",
      "state": "OH",
      "postal_code": "43123-1895",
      "additional_info_contact": "614-317-1909",
      "reason_for_recall": "This recall has been initiated due to a potential malfunction of the photo interrupter (Pl). The potential\nmalfunction has been attributed to aging and premature deterioration of the Pl collector current.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Customers were sent a recall notification by email on July 11, 2017 informing them that their local Field Service Engineer would contact them to make arrangements to proactively replace the affected parts. Follow up notifications will be by Federal Express with verification of delivery.",
      "product_quantity": "565 total devices U.S.",
      "distribution_pattern": "Worldwide Distribution - U.S. Nationwide - Latin America",
      "openfda": {
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        ],
        "device_name": "Fluorometer, For Clinical Use",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.2560",
        "device_class": "1"
      }
    }
  ]
}