ABL800 Flex Analyzer recall in Canada: inaccurate creatinine measurements
In plain language
This recall involves the ABL800 Flex Analyzer sold in Canada. It's being recalled because it may provide inaccurate creatinine measurements, which could lead to incorrect diagnoses of kidney function. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model number 393-801.
- Contact Radiometer Medical Aps for further instructions.
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Affected products
ABL800 Flex Analyzer
Model: 393-801
Lot: All serial numbers
Why this matters
Inaccurate medical measurements
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 serial numbers
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 393-801
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?
Inaccurate medical measurements
What should consumers do?
Stop using the product immediately. Check model number 393-801. Contact Radiometer Medical Aps for further instructions.
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. Inaccurate medical measurements
When was this product recalled?
This product was recalled on July 5, 2018.