Atellica CI System recall in Canada: Inaccurate test results
In plain language
This recall involves the Atellica CI System, a medical device used in healthcare settings. It's being recalled because it may provide inaccurate sodium, potassium, and chloride test results. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer, Siemens Healthcare Diagnostics Inc., for additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Atellica CI System
Model: 10947347
Lot: IRC009062411, IRC007512342, IRC009012411
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: IRC009062411, IRC007512342, IRC009012411
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10947347
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?
Contact the manufacturer, Siemens Healthcare Diagnostics Inc., for 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 results
When was this product recalled?
This product was recalled on November 15, 2024.
Is the Siemens Healthcare Diagnostics Inc. brand affected by this recall?
Yes, Siemens Healthcare Diagnostics Inc. products are affected by this recall. This recall involves the Atellica CI System, a medical device used in healthcare settings. It's being recalled because it may provide inaccurate sodium, potassium, and chloride test results. Healthcare professionals should contact the manufacturer for more information.