ARKON Anesthesia Delivery System recall in Canada: loss of ventilation
In plain language
This recall involves the ARKON Anesthesia Delivery System sold in Canada. It's being recalled because the system can fail during use, leading to a loss of mechanical ventilation and monitoring. Healthcare professionals should stop using affected units and follow the instructions in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers ARKN-000005 and ARKN-000015.
- Follow the return or repair instructions from Spacelabs Healthcare Ltd.
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Affected products
ARKON Anesthesia Delivery System
Model: ARKN-000005, ARKN-000015
Why this matters
Loss of mechanical ventilation and monitoring
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 model number
Model numbers are typically on the product label or packaging.
Affected models: ARKN-000005, ARKN-000015
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?
Loss of mechanical ventilation and monitoring
What should consumers do?
Stop using the product immediately. Check model numbers ARKN-000005 and ARKN-000015. Follow the return or repair instructions from Spacelabs Healthcare Ltd.
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. Loss of mechanical ventilation and monitoring
When was this product recalled?
This product was recalled on August 17, 2018.
Is the ARKON brand affected by this recall?
Yes, ARKON products are affected by this recall. This recall involves the ARKON Anesthesia Delivery System sold in Canada. It's being recalled because the system can fail during use, leading to a loss of mechanical ventilation and monitoring. Healthcare professionals should stop using affected units and follow the instructions in the official notice.