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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 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.
Recall announced
September 11, 2025
Reported by FDA DEVICE
October 22, 2025
RecallRadar source check
April 18, 2026
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
- Verify model BF-1TQ170
- 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
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Safety Guide
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