VITROS XT 7600 Integrated System recall in Canada: inaccurate test results
In plain language
This recall involves the VITROS XT 7600 Integrated System, a medical device used in healthcare settings. It's being recalled because it may dispense an incorrect sample volume without alerting the operator, leading to inaccurate test results. Healthcare professionals should stop using affected units and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and serial numbers.
- Follow the instructions from Ortho Clinical Diagnostics Inc. for return or repair.
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Affected products
VITROS XT 7600 Integrated System
Model: 684 4461
Lot: J76000142, J76000143
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: J76000142, J76000143
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 684 4461
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?
Stop using the product immediately. Check the model and serial numbers. Follow the instructions from Ortho Clinical Diagnostics Inc. for return or repair.
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 March 22, 2019.
Is the VITROS brand affected by this recall?
Yes, VITROS products are affected by this recall. This recall involves the VITROS XT 7600 Integrated System, a medical device used in healthcare settings. It's being recalled because it may dispense an incorrect sample volume without alerting the operator, leading to inaccurate test results. Healthcare professionals should stop using affected units and follow the return steps in the official notice.