ABL90 Flex and Flex Plus recall in Canada: Performance issue
In plain language
This recall involves ABL90 Flex and ABL90 Flex Plus medical devices sold in Canada. They are being recalled because the analyzer software may unexpectedly freeze during a sample measurement. This could result in a lost sample.
What to do
- Contact the manufacturer, Radiometer Medical Aps, for additional information.
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Affected products
ABL90 Flex Plus
Model: 393-092
ABL90 Flex
Model: 393-090
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: 393-090, 393-092
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 ABL90 Flex and ABL90 Flex Plus medical devices sold in Canada. They are being recalled because the analyzer software may unexpectedly freeze during a sample measurement. This could result in a lost sample.
What should consumers do?
Contact the manufacturer, Radiometer Medical Aps, for 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?
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 March 25, 2025.
Is the Radiometer Medical Aps brand affected by this recall?
Yes, Radiometer Medical Aps products are affected by this recall. This recall involves ABL90 Flex and ABL90 Flex Plus medical devices sold in Canada. They are being recalled because the analyzer software may unexpectedly freeze during a sample measurement. This could result in a lost sample.