🔍 RecallPedia

EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190

Class I - Dangerous
🏥 Medical Devices Recalled: September 11, 2025 Olympus Corporation of the Americas Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model No. BF-P190; UDI: 4953170342110; All Serial No.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Olympus Corporation of the Americas
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190

Product Codes/Lot Numbers:

Model No. BF-P190; UDI: 4953170342110; All Serial No.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0057-2026

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