Centricity Universal Viewer recall in Canada: incorrect patient images
In plain language
This recall involves the Centricity Universal Viewer medical device sold in Canada. It's being recalled because an error can cause incorrect patient images to be displayed. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model number 2088034-X and lot number 2090255-001.
- Contact GE Healthcare for further instructions.
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Affected products
Centricity Universal Viewer
Model: 2088034-X
Lot: 2090255-001
Why this matters
Incorrect patient images displayed
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: 2090255-001
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 2088034-X
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?
Incorrect patient images displayed
What should consumers do?
Stop using the product immediately. Check model number 2088034-X and lot number 2090255-001. Contact GE Healthcare 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. Incorrect patient images displayed
When was this product recalled?
This product was recalled on November 2, 2018.
Is the Centricity brand affected by this recall?
Yes, Centricity products are affected by this recall. This recall involves the Centricity Universal Viewer medical device sold in Canada. It's being recalled because an error can cause incorrect patient images to be displayed. Stop using the product and follow the return/repair steps in the official notice.