Olympus Bronchovideoscope F-1TQ180 Recalled for Instrument Channel Port Loosening
Olympus is recalling 1,134 Bronchovideoscope F-1TQ180 units because attaching non-Olympus accessories may cause the instrument channel port to loosen.
What this means for you
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, and the source text describes a mechanical defect (loosening port) without reporting any specific injuries, illnesses, or fatalities, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Olympus Corporation of the Americas is recalling 1,134 units of the Bronchovideoscope F-1TQ180. The recall covers all lot codes for this specific model. The products were 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 can lead to the loosening of the instrument channel port.
Healthcare facilities and consumers who have this device should stop using it and contact Olympus Corporation of the Americas for further instructions on how to proceed.
The recalled product
- Product
- Bronchovideoscope F-1TQ180
- Manufacturer
- Olympus Corporation of the Americas
- Category
- Medical Device — Endoscopy
- Hazard
- Affected units
- 1,134
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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