FDAClass IIJanuary 17, 2024

Model No. BF-P190 recall

Model No. BF-P190, EVIS EXERA III Bronchovideoscope

Why was Model No. BF-P190 recalled?

Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 04953170342110 All serial numbers

Product
Model No. BF-P190, EVIS EXERA III Bronchovideoscope
Recalling firm
Shirakawa Olympus Co., Ltd.
Quantity
2600 US; 3214 OUS
Distribution
US Nationwide distribution.
Recall date
January 17, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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