healthRecalled on Nov 3, 2025

Olympus Bronchofiberscopes and bronchovideoscopes

Sold At: Olympus Corporation

Source: FDA-ALERT

Olympus Bronchofiberscopes and bronchovideoscopes

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Summary

CENTER VALLEY, Pa., (October 31, 2025) – Olympus Corporation has announced a voluntary, global medical device corrective action to provide further clarification on the safe and effective use of bronchoscopes with laser therapy, argon plasma coagulation or high-frequency cauterization equipment during therapeutic procedures within the tracheobronchial tree. This corrective action supersedes the previous related communication in 2023 to address adverse event complaints of endobronchial combustion involving therapeutic instruments with Olympus bronchoscopes, which included one death. Since the Field Corrective Action in 2023, Olympus conducted additional assessment on the use of bronchoscopes with laser therapy, argon plasma coagulation, and high-frequency cauterization equipment. Through these investigations of clinical conditions, Olympus determined that additional updates to the instructions for use are necessary. Since 2023, Olympus has received reports of four additional incidents involving serious injury, including one from the U.S.

What to do next

  • 1Stop using this product immediately
  • 2Contact Olympus Corporation for return or refund information
  • 3Check with your retailer for recall status and remedy options
  • 4Visit the official FDA recall page for complete details

Summaries only; always follow the official notice.