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Olympus BF-1TQ170 Bronchoscope Recall Expanded for IFU Clarifications

Olympus Corporation of the Americas recalls the BRONCHOVIDEOSCOPE BF-1TQ170. The recall is active with 2,092 units in the outside US market and no US units affected. The action seeks updated instructions for safe use with laser and high-frequency therapy equipment. Healthcare providers should stop use and follow manufacturer recall instructions.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
September 11, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
September 11, 2025
Hazard Level
HIGH
Brand
Olympus Corporation of the Americas
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Olympus Corporation of the Americas
Product type
Bronchoscope
Model numbers
BF-1TQ170, UDI: 4953170342943
Sold at
Unknown
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    September 11, 2025

  2. Reported by FDA DEVICE

    October 22, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Olympus Corporation of the Americas or your healthcare provider for instructions

About This Product

Bronchoscopes are used to view and diagnose airways via a flexible scope. They can be used with adjunct devices such as laser or energy-based therapy equipment during procedures.

Why This Is Dangerous

The recall addresses added IFU updates to clarify safe and effective use when used with laser, argon plasma coagulation, and high-frequency therapy equipment. The risk is linked to procedural safety rather than a device failure alone.

Industry Context

This recall is not presented as part of a broader industry pattern in the notice.

Real-World Impact

Health care providers may need to adjust procedural guidelines. The recall emphasizes strict adherence to updated IFU when using adjunct devices during bronchoscopy.

Practical Guidance

How to identify if yours is affected

  1. Verify model BF-1TQ170
  2. Confirm all serial numbers are affected

Where to find product info

Refer to the official FDA recall page for BF-1TQ170 IFU update guidance and device identification details.

What timeline to expect

Remedies and updated instructions will be communicated by Olympus; no specific timetable is provided.

If the manufacturer is unresponsive

  • Escalate to healthcare institution's compliance officer
  • Request guidance from Olympus customer support or distributor

How to prevent similar issues

  • Always use updated IFU with any bronchoscopic procedure involving laser or energy-based devices
  • Ensure equipment compatibility before procedures
  • Maintain documentation of updated safety communications

Documentation advice

Keep a copy of the recall notice, IFU update communications, and any correspondence with Olympus.

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Product Details

Product: BRONCHOVIDEOSCOPE BF-1TQ170. Brand: Olympus. Classification: Class I. Quantity: 0 US units; 2,092 OUS units. Distribution: US Nationwide Distribution. Status: Active recall as of 2025-09-11.

Reported Incidents

No incident or injury count is provided in the recall notice. The hazard level is rated HIGH, but no specific injuries are reported in the document.

Key Facts

  • BF-1TQ170 model
  • All serial numbers affected
  • 0 US units recalled; 2,092 outside US

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
BF-1TQ170
UDI: 4953170342943
Affected States
ALL
Report Date
October 22, 2025
Recall Status
ACTIVE

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