{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3500 Corporate Pkwy",
      "reason_for_recall": "Issuance of validated, new reprocessing procedures.   This corrective action is being undertaken as a result of ongoing manufacturer and FDA activities relating to reported patient infections associated with  duodenoscopes.  The new cleaning procedure requires additional recess flushing and forceps elevator raising/lowering steps during precleaning, manual cleaning and manual disinfection.",
      "address_2": "PO Box 610",
      "product_quantity": "994",
      "code_info": "All",
      "center_classification_date": "20180621",
      "distribution_pattern": "Nationwide",
      "state": "PA",
      "product_description": "Olympus JF-140F duodenoscopes (Model NumberJF-140F)",
      "report_date": "20180627",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus Corporation of the Americas",
      "recall_number": "Z-2269-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79998",
      "termination_date": "20200505",
      "recall_initiation_date": "20180511",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}