Remisol Advance recall in Canada: database error
In plain language
This recall involves Remisol Advance medical devices sold in Canada. It's being recalled because a database error could cause test results to be duplicated and linked to the wrong patient. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers: Version 1.6, 1.7, 1.8, 1.9.
- Contact Beckman Coulter for instructions.
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Affected products
Remisol Advance
Model: VERSION 1.6, VERSION 1.7, VERSION 1.8, VERSION 1.9
Lot: All lots
Why this matters
Incorrect medical information
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 lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: VERSION 1.6, VERSION 1.7, VERSION 1.8, VERSION 1.9
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 medical information
What should consumers do?
Stop using the product immediately. Check model numbers: Version 1.6, 1.7, 1.8, 1.9. Contact Beckman Coulter for 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. Incorrect medical information
When was this product recalled?
This product was recalled on October 3, 2019.
Is the Remisol Advance brand affected by this recall?
Yes, Remisol Advance products are affected by this recall. This recall involves Remisol Advance medical devices sold in Canada. It's being recalled because a database error could cause test results to be duplicated and linked to the wrong patient. Stop using the product and follow the return steps in the official notice.