Olympus Recalls Bronchovideoscope BF-MP60 Due to Port Loosening Risk
Olympus is recalling 653 Bronchovideoscope BF-MP60 units because non-Olympus accessories may cause the instrument channel port to loosen.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device with a structural defect (loosening port) that poses a risk of harm during use, but the source text does not report any specific injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Olympus Corporation of the Americas is recalling 653 units of the Bronchovideoscope BF-MP60. 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.
The affected products were distributed nationwide in the United States and in Canada. The recall covers all lot codes for this specific model. No specific dates or additional distribution details are provided in the source text.
Healthcare facilities and consumers should stop using the affected Bronchovideoscope BF-MP0 units immediately. Users should contact Olympus Corporation of the Americas for instructions on how to return the device or obtain a replacement, as per standard recall procedures.
The recalled product
- Product
- Bronchovideoscope BF-MP60
- Manufacturer
- Olympus Corporation of the Americas
- Category
- Medical Device — Endoscopy
- Affected units
- 653
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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