Aizu Olympus Co., Ltd. 2022-08-31 Health serious FDA
Health · FDA · Recall #FDA-Z-1559-2022
EVIS EXERA III Bronchovideoscope Recall
Issued August 31, 2022 · Aizu Olympus Co., Ltd.
In August 2022, Aizu Olympus Co., Ltd. recalled the EVIS EXERA III Bronchovideoscope, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
What you should do
- 1 Stop using EVIS EXERA III Bronchovideoscope right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Aizu 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
- Aizu Olympus Co., Ltd.
- Category
- Health
- Recall date
- August 31, 2022
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of FL, IL, NC, PA & TX.
- Recall number
- FDA-Z-1559-2022
- Made in
- Japan
- Issuing agency
- FDA
In context
- Aizu Olympus Co., Ltd. has 4 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.