Intesys Clinical Suite (ICS) G2 recall in Canada: incorrect patient data
In plain language
This recall involves the Intesys Clinical Suite (ICS) G2 - Smart Disclosure medical device sold in Canada. It's being recalled because it may print patient waveforms with incorrect patient data. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for more information.
- Follow the instructions from Spacelabs Healthcare Inc.
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Affected products
Intesys Clinical Suite (ICS) G2 - Smart Disclosure
Model: 92810
Lot: More than 100 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 100 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 92810
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 immediately. Contact the manufacturer for more information. Follow the instructions from Spacelabs Healthcare Inc.
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 22, 2019.