ABL90 FLEX - Analyzer recall in Canada: incorrect measurements
In plain language
This recall involves the ABL90 FLEX - Analyzer sold in Canada. It's being recalled because it may provide incorrect measurements for several parameters. This could lead to misdiagnosis or incorrect treatment for patients. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
ABL90 FLEX - Analyzer
Model: 393-090
Lot: Version 3.3 MR1 or lower
Why this matters
Incorrect measurements leading to misdiagnosis
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: Version 3.3 MR1 or lower
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 393-090
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 measurements leading to misdiagnosis
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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 measurements leading to misdiagnosis
When was this product recalled?
This product was recalled on June 22, 2018.