Cortrak*2 Enteral Access System recall in Canada: misplacement risk
In plain language
This recall involves the Cortrak*2 Enteral Access System (EAS) sold in Canada. It's being recalled because of labeling modifications related to misplacement of feeding tubes. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer if you require additional information.
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Affected products
Cortrak*2 Enteral Access System (Eas)
Model: 20-0950 (UDI 00350770472010), 20-0950 (UDI 10680651472011), P20-0950 (UDI 00350770472065), P20-0950 (UDI 10680651472066)
Lot: All lots
Why this matters
Misplacement risk for feeding tubes
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: 20-0950 (UDI 00350770472010), 20-0950 (UDI 10680651472011), P20-0950 (UDI 00350770472065), P20-0950 (UDI 10680651472066)
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?
Misplacement risk for feeding tubes
What should consumers do?
Stop using the product immediately. Contact the manufacturer if you require 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?
Yes, there may be a health risk. Misplacement risk for feeding tubes
When was this product recalled?
This product was recalled on April 19, 2022.
Is the Avanos Medical, Inc. brand affected by this recall?
Yes, Avanos Medical, Inc. products are affected by this recall. This recall involves the Cortrak*2 Enteral Access System (EAS) sold in Canada. It's being recalled because of labeling modifications related to misplacement of feeding tubes. Stop using the product and follow the return/repair steps in the official notice.