ABL90 FLEX - Analyzer recall in Canada: delayed medical treatment
In plain language
This recall involves the ABL90 FLEX - Analyzer, a medical device used in Canada. It's being recalled because a software vulnerability could cause the device to shut down or reboot, leading to delayed medical treatment. 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: Softw. version:RXPE v1.3xxxxxx
Why this matters
Delayed medical treatment
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: Softw. version:RXPE v1.3xxxxxx
- 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?
Delayed medical treatment
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. Delayed medical treatment
When was this product recalled?
This product was recalled on July 19, 2019.