ATELLICA CH 930 ANALYZER (2019-08-01)
In plain language
This recall involves the ATELLICA CH 930 ANALYZER medical device sold in Canada. It's being recalled because it may report incorrect serum indices for Hemolysis and Lipemia. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
ATELLICA CH 930 ANALYZER
Model: 11067000
Lot: CM00237, CM00238, CM00239, CM00416, CM01054, CM01112, CM01178
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: CM00237, CM00238, CM00239, CM00416, CM01054, CM01112, CM01178
- 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?
This recall involves the ATELLICA CH 930 ANALYZER medical device sold in Canada. It's being recalled because it may report incorrect serum indices for Hemolysis and Lipemia. Stop using the product and follow the return/repair steps in the official notice.
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on August 9, 2019.