EVIS EXERA III Duodenovideoscope recall in Canada: labelling and packaging issue
In plain language
This recall involves the EVIS EXERA III Duodenovideoscope sold in Canada. It's being recalled because of an issue with its labelling and packaging related to cleaning instructions. This recall is for healthcare professionals.
What to do
- Contact the manufacturer for additional information.
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Affected products
EVIS EXERA III Duodenovideoscope
Model: TJF-Q190V
Lot: All lots.
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: TJF-Q190V
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves the EVIS EXERA III Duodenovideoscope sold in Canada. It's being recalled because of an issue with its labelling and packaging related to cleaning instructions. This recall is for healthcare professionals.
What should consumers do?
Contact the manufacturer for additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on May 22, 2025.
Is the OLYMPUS MEDICAL SYSTEMS CORP. brand affected by this recall?
Yes, OLYMPUS MEDICAL SYSTEMS CORP. products are affected by this recall. This recall involves the EVIS EXERA III Duodenovideoscope sold in Canada. It's being recalled because of an issue with its labelling and packaging related to cleaning instructions. This recall is for healthcare professionals.