Olympus Bronchovidescope BF-1T240 Recalled Due to Instrument Channel Port Loosening
Olympus is recalling 1,605 Bronchovidescope BF-1T240 units because attaching non-Olympus accessories may have loosened the instrument channel port.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically indicates a situation where use of the product may cause temporary or medically reversible health consequences. No specific injuries or illnesses are reported in the source text, and the hazard is a mechanical defect (loosening) rather than a direct biological or electrical safety failure.
Plain-English summary
Olympus Corporation of the Americas is recalling 1,605 units of the Bronchovidescope BF-1T240. The recall covers all lot codes and includes products distributed nationwide in the United States and in Canada.
The recall was initiated because the attachment of non-Olympus accessories to the bronchoscope's instrument channel port may have resulted in more applied force than expected. This excessive force may have led to the loosening of the instrument channel port.
Healthcare facilities and users should stop using the affected devices and contact Olympus Corporation of the Americas for further instructions on the recall.
The recalled product
- Product
- Bronchovidescope BF-1T240
- Manufacturer
- Olympus Corporation of the Americas
- Category
- Medical Device — Endoscopy
- Hazard
- Affected units
- 1,605
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- all lot codes
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 30 recalled by Olympus Corporation of the Americas under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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