Atellica Ch 930 Analyzer recall in Canada: software defect
In plain language
This recall involves the Atellica Ch 930 Analyzer, a medical device, sold in Canada. It's being recalled because of a software defect that could lead to incorrect patient sample results. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Atellica Ch 930 Analyzer
Model: 11067000
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Potential for erroneous patient sample 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: 11067000
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?
Potential for erroneous patient sample 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. Potential for erroneous patient sample results
When was this product recalled?
This product was recalled on December 7, 2021.
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 Ch 930 Analyzer, a medical device, sold in Canada. It's being recalled because of a software defect that could lead to incorrect patient sample results. Contact the manufacturer for more information.