Cortrak 2 Enteral Access System recall in Canada: Unauthorized device
In plain language
This recall involves the Cortrak 2 Enteral Access System sold in Canada. It's being recalled because it is an unauthorized medical device. Healthcare professionals should stop using the product until the licensing issue is resolved.
What to do
- Stop using the product immediately.
- Check for model number P20-0950 or 20-0950.
- Discontinue use until the licence issue has been resolved.
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Affected products
Cortrak 2 Enteral Access System
Model: 20-0950, P20-0950
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: 20-0950, P20-0950
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 Cortrak 2 Enteral Access System sold in Canada. It's being recalled because it is an unauthorized medical device. Healthcare professionals should stop using the product until the licensing issue is resolved.
What should consumers do?
Stop using the product immediately. Check for model number P20-0950 or 20-0950. Discontinue use until the licence issue has been resolved.
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 June 7, 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 sold in Canada. It's being recalled because it is an unauthorized medical device. Healthcare professionals should stop using the product until the licensing issue is resolved.