STA - ImmunoDef VIII and STA-Deficient VIII (2020-03-05)
In plain language
This recall involves STA ImmunoDef VIII and STA-Deficient VIII medical devices sold in Canada. They are being recalled because they may give inaccurate test results for Factor VIII assays. Stop using the products and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for more information.
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Affected products
STA - ImmunoDef VIII
Model: 728
Lot: More than 10 numbers, contact manufacturer.
STA - Deficient VIII
Model: 725
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Inaccurate 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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 725, 728
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?
Inaccurate test results
What should consumers do?
Stop using the product immediately. Contact the manufacturer for more information.
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. Inaccurate test results
When was this product recalled?
This product was recalled on April 15, 2020.
Is the STA brand affected by this recall?
Yes, STA products are affected by this recall. This recall involves STA ImmunoDef VIII and STA-Deficient VIII medical devices sold in Canada. They are being recalled because they may give inaccurate test results for Factor VIII assays. Stop using the products and contact the manufacturer for more information.