Checkcell® recall in Canada: Sterility issue
In plain language
This recall involves Checkcell® medical devices sold in Canada. They are being recalled because some vials showed signs of fungal growth, which affects sterility. This recall is for healthcare professionals. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check lot number 43257.
- Return the affected product as instructed.
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Affected products
Checkcell®
Model: 0002224, 0002225
Lot: 43257
Why this matters
Sterility issue due to fungal growth
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: 43257
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 0002224, 0002225
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?
Sterility issue due to fungal growth
What should consumers do?
Stop using the product immediately. Check lot number 43257. Return the affected product 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. Sterility issue due to fungal growth
When was this product recalled?
This product was recalled on December 30, 2025.
Is the Immucor Inc. brand affected by this recall?
Yes, Immucor Inc. products are affected by this recall. This recall involves Checkcell® medical devices sold in Canada. They are being recalled because some vials showed signs of fungal growth, which affects sterility. This recall is for healthcare professionals. Stop using the product and follow the return steps in the official notice.