{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3500 Corporate Pkwy.",
      "reason_for_recall": "Olympus initiated a software upgrade and enhancement in 2009 and completed the action in 2010.  The upgrade and enhancement were initiated due to complaints of overheating, smoke vapors and failure to operate associated with the Olympus SurgMaster electrosurgical unit, model UES-40 (\"UES-40\") when used in conjunction with the Olympus WA22557C electrode.  The complaint investigations revealed that",
      "address_2": "P.O. Box 610",
      "product_quantity": "608",
      "code_info": "Model UES-40, all serial numbers prior to 7925334 that have not been upgraded.",
      "center_classification_date": "20130508",
      "distribution_pattern": "Nationwide Distribution - USA Nationwide including the states of: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, UT, VA, WA, WV, and WY.",
      "state": "PA",
      "product_description": "Olympus SurgMaster UES-40 electrosurgical unit (\"UES-40\")    Product Usage:  Designed for use in a medical facility under the supervision of a trained physician. It has been designed for general (open) and endoscopic surgery including urology, gynecology, respiratory and gastroenterology in conjunction with Olympus designed electrosurgical accessories, endoscopes (fiberscopes, videoscopes and rigid scopes) applicable for electrosurgery (cutting and coagulation), light sources and other ancillary equipment.",
      "report_date": "20130515",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus America Inc.",
      "recall_number": "Z-1277-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64935",
      "termination_date": "20130705",
      "recall_initiation_date": "20091110",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}