UniCel DxC medical devices recall in Canada: calibration failure
In plain language
This recall involves UniCel DxC 600, 600i, 800, 800i, 860i, and 880i medical devices sold in Canada. It's being recalled because chloride electrode tips may fail calibration span. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and lot numbers.
- Contact Beckman Coulter for more information.
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Affected products
UniCel DxC 600
Model: 4764
Lot: ELECTRODE TIP LOTS 1822 & 1827
UniCel DxC 800
Model: 4764
Lot: ELECTRODE TIP LOTS 1822 & 1827
UniCel DxC 600i
Model: 4767
Lot: ELECTRODE TIP LOTS 1822 & 1827
UniCel DxC 880i (Part of DxC 800i integrated system)
Model: 4767
Lot: ELECTRODE TIP LOTS 1822 & 1827
UniCel DxC 860i (Part of DxC 800i integrated system)
Model: 4767
Lot: ELECTRODE TIP LOTS 1822 & 1827
Why this matters
Calibration failure
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: ELECTRODE TIP LOTS 1822 & 1827
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 4764, 4767
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?
Calibration failure
What should consumers do?
Stop using the product immediately. Check model and lot numbers. Contact Beckman Coulter for more 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. Calibration failure
When was this product recalled?
This product was recalled on February 15, 2019.
Is the UniCel DxC brand affected by this recall?
Yes, UniCel DxC products are affected by this recall. This recall involves UniCel DxC 600, 600i, 800, 800i, 860i, and 880i medical devices sold in Canada. It's being recalled because chloride electrode tips may fail calibration span. Stop using the product and follow the return/repair steps in the official notice.