PreciseType and RHD Molecular BeadChip Tests recall in Canada: incorrect results
In plain language
This recall involves PreciseType HEA Molecular BeadChip Test and RHD Molecular BeadChip Test sold in Canada. They are being recalled because a component may not work correctly, which could lead to incorrect test results. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Contact Immucor for a replacement Clean-up Reagent.
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Affected products
PreciseType HEA Molecular BeadChip Test
Model: 800-20202-08
Lot: 19-21-V
RHD Molecular BeadChip Test
Model: 800-10220-48
Lot: 19-28-C
Why this matters
Incorrect test 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: 19-21-V, 19-28-C
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 800-10220-48, 800-20202-08
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 test results
What should consumers do?
Stop using the product immediately. Check model and lot numbers. Contact Immucor for a replacement Clean-up Reagent.
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 test results
When was this product recalled?
This product was recalled on November 28, 2018.