SYNCHRON Systems ISE Electrolyte Reference recall in Canada: false results
In plain language
This recall involves SYNCHRON Systems ISE Electrolyte Reference sold in Canada. It's being recalled because it may cause CO2 calibration failures, high CO2 quality control recoveries, and false high patient results. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check lot number M909206.
- Contact Beckman Coulter for further instructions.
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Affected products
SYNCHRON Systems ISE Electrolyte Reference
Model: A28937
Lot: M909206
Why this matters
False patient 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: M909206
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: A28937
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?
False patient results
What should consumers do?
Stop using the product immediately. Check lot number M909206. Contact Beckman Coulter for further instructions.
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. False patient results
When was this product recalled?
This product was recalled on February 28, 2020.
Is the SYNCHRON Systems brand affected by this recall?
Yes, SYNCHRON Systems products are affected by this recall. This recall involves SYNCHRON Systems ISE Electrolyte Reference sold in Canada. It's being recalled because it may cause CO2 calibration failures, high CO2 quality control recoveries, and false high patient results. Stop using the product and follow the return/repair steps in the official notice.