Hemochron® Jr. recall in Canada: Foreign object hazard
In plain language
This recall involves the Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette sold in Canada. It's being recalled because a foreign object (single edge blade) was found inside a test cartridge. The manufacturer will contact customers directly regarding this issue.
What to do
- Stop using the product immediately.
- Check the model and lot number: JACT-LR and E5JLR132.
- Follow instructions from the manufacturer.
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Affected products
Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette
Model: JACT-LR
Lot: E5JLR132
Why this matters
Foreign object hazard
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: E5JLR132
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: JACT-LR
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?
Foreign object hazard
What should consumers do?
Stop using the product immediately. Check the model and lot number: JACT-LR and E5JLR132. Follow instructions from 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. Foreign object hazard
When was this product recalled?
This product was recalled on November 13, 2025.
Is the Accriva Diagnostics, Inc. brand affected by this recall?
Yes, Accriva Diagnostics, Inc. products are affected by this recall. This recall involves the Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette sold in Canada. It's being recalled because a foreign object (single edge blade) was found inside a test cartridge. The manufacturer will contact customers directly regarding this issue.