{
  "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": "2026-08-27",
    "results": {
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      "product_res_number": "Z-0754-2017",
      "event_date_initiated": "2016-11-03",
      "event_date_created": "2016-12-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2019-02-06",
      "res_event_number": "75601",
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      "firm_fei_number": "2429304",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "PO Box 610",
      "city": "Center Valley",
      "state": "PA",
      "postal_code": "18034-0610",
      "additional_info_contact": "Laura Storms\n484-8965688",
      "reason_for_recall": "Software malfunction that results in incorrect generation or display of error codes.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Olympus mailed on 11/03/2016 an Urgent Communication Letter to customers affected by the recall.  The letter requested that consignees inspect their inventory for the affected lots and call Customer Service to obtain a Returned Material Authorization (RMA) to return the product.",
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