Shirakawa Olympus Co., Ltd. 2024-01-17 Health serious FDA
Health · FDA · Recall #FDA-Z-0691-2024
Model No. CYF-V2, VISERA Cysto-Nephro Videoscope Recall
Issued January 17, 2024 · Shirakawa Olympus Co., Ltd.
In January 2024, Shirakawa Olympus Co., Ltd. recalled the Model No. CYF-V2, VISERA Cysto-Nephro Videoscope, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
What you should do
- 1 Stop using Model No. CYF-V2, VISERA Cysto-Nephro Videoscope right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Shirakawa Olympus Co., Ltd. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Shirakawa Olympus Co., Ltd.
- Category
- Health
- Recall date
- January 17, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-0691-2024
- Made in
- Japan
- Issuing agency
- FDA
In context
- Shirakawa Olympus Co., Ltd. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.