AQUIOS CL Flow Cytometer System recall in Canada: sample misidentification
In plain language
This recall involves the AQUIOS CL Flow Cytometer System used in Canada. It's being recalled because specific steps can lead to sample misidentification and incorrect results. Healthcare professionals should stop using the product and follow the instructions in the official notice.
What to do
- Stop using the AQUIOS CL Flow Cytometer System immediately if the described sequence of events is followed.
- Refer to the official recall notice for detailed instructions.
- Ensure proper procedures are followed to prevent sample misidentification.
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Affected products
AQUIOS CL Flow Cytometer System
Model: B30166
Lot: SOFTWARE VERSION 2
Why this matters
Sample misidentification and erroneous results
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: SOFTWARE VERSION 2
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: B30166
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?
Sample misidentification and erroneous results
What should consumers do?
Stop using the AQUIOS CL Flow Cytometer System immediately if the described sequence of events is followed. Refer to the official recall notice for detailed instructions. Ensure proper procedures are followed to prevent sample misidentification.
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. Sample misidentification and erroneous results
When was this product recalled?
This product was recalled on March 2, 2018.