Centricity™ Universal Viewer Zero Footprint Client
In plain language
This recall involves the Centricity Universal Viewer Zero Footprint Client, used in healthcare settings. It's being recalled because it may show the wrong patient's timeline. Healthcare providers should contact the manufacturer for more information.
What to do
- Stop using the product if you are a healthcare provider.
- Contact the manufacturer for additional information.
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Affected products
Centricity™ Universal Viewer Zero Footprint Client
Model: 00840682102988
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Incorrect patient data
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 00840682102988
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 data
What should consumers do?
Stop using the product if you are a healthcare provider. Contact the manufacturer for additional 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. Incorrect patient data
When was this product recalled?
This product was recalled on February 5, 2026.
Is the GE HEALTHCARE brand affected by this recall?
Yes, GE HEALTHCARE products are affected by this recall. This recall involves the Centricity Universal Viewer Zero Footprint Client, used in healthcare settings. It's being recalled because it may show the wrong patient's timeline. Healthcare providers should contact the manufacturer for more information.