Immulite 2000 System recall in Canada: inaccurate test results
In plain language
This recall involves the Immulite 2000 System-Human Chorionic Gonadotropin (HCG) Assay sold in Canada. It's being recalled because it may provide inaccurate test results. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Immulite 2000 System-Human Chorionic Gonadotropin (HCG) Assay
Model: L2KCG2, L2KCG6
Lot: 466, 463
Why this matters
Inaccurate test or measurement 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: 466, 463
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: L2KCG2, L2KCG6
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 or measurement results
What should consumers do?
Contact the manufacturer if you require additional 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 or measurement results
When was this product recalled?
This product was recalled on March 28, 2022.
Is the Siemens Healthcare Diagnostics Products Limited brand affected by this recall?
Yes, Siemens Healthcare Diagnostics Products Limited products are affected by this recall. This recall involves the Immulite 2000 System-Human Chorionic Gonadotropin (HCG) Assay sold in Canada. It's being recalled because it may provide inaccurate test results. Contact the manufacturer for more information.