Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0056-2026 — EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180

U.S. FDA — Device Enforcement · United States · 2025-09-11 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0056-2026
Date of alert
2025-09-11
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Olympus Corporation of the Americas
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4953170339288
Reported risk: Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.