AZURION 7 M20 recall in Canada: incorrect display during medical procedures
In plain language
This recall involves the AZURION 7 M20 medical device used in Canada. It's being recalled because it may display incorrect information during live guidance in medical procedures. Healthcare professionals should follow the instructions in the official notice.
What to do
- Stop using the product immediately if the L-arm is not repositioned.
- Check model number 722 079.
- Follow the return/repair steps in the official notice.
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Affected products
AZURION 7 M20
Model: 722 079
Lot: Not applicable
Why this matters
Incorrect display 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: Not applicable
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 722 079
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?
Incorrect display during medical procedures
What should consumers do?
Stop using the product immediately if the L-arm is not repositioned. Check model number 722 079. Follow the return/repair steps in the official notice.
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. Incorrect display during medical procedures
When was this product recalled?
This product was recalled on May 1, 2020.
Is the AZURION brand affected by this recall?
Yes, AZURION products are affected by this recall. This recall involves the AZURION 7 M20 medical device used in Canada. It's being recalled because it may display incorrect information during live guidance in medical procedures. Healthcare professionals should follow the instructions in the official notice.