Duodenoscope recall in Canada: detachment risk
In plain language
This recall involves Duodenoscopes (model ED-580XT) used in medical procedures in Canada. They are being recalled because the disposable distal end cap can detach during use. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers: ED-580XT.
- Contact the manufacturer for return or repair instructions.
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Affected products
Duodenoscope
Model: ED-580XT
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Detachment risk during medical procedures
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: ED-580XT
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?
Detachment risk during medical procedures
What should consumers do?
Stop using the product immediately. Check model numbers: ED-580XT. Contact the manufacturer for return or repair instructions.
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?
Yes, there may be a health risk. Detachment risk during medical procedures
When was this product recalled?
This product was recalled on May 29, 2020.