ABL800 Analyzers recall in Canada: Patient mix-up risk
In plain language
This recall involves ABL800 Analyzers used in Canada. They are being recalled because a software issue could lead to patient data being incorrectly assigned to samples. This could cause patient mix-ups during medical testing.
What to do
- Stop using the product immediately.
- Contact the manufacturer for more information.
- Follow the instructions provided by the manufacturer.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
ABL800 Analyzers
Model: 393-800, 393-801
Lot: More than 100 numbers, contact manufacturer.
Why this matters
Patient mix-up risk
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: More than 100 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 393-800, 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?
Patient mix-up risk
What should consumers do?
Stop using the product immediately. Contact the manufacturer for more information. Follow the instructions provided by the manufacturer.
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. Patient mix-up risk
When was this product recalled?
This product was recalled on July 5, 2018.