Hybrid Recon 4.0 and 5.0 recall in Canada: Performance issue
In plain language
This recall involves Hybrid Recon 4.0 and 5.0 medical devices. They are being recalled because of a performance issue where aspect and CT series may not align correctly. This could lead to incorrect alignment during reconstruction of studies. This recall is intended for the healthcare industry.
What to do
- Contact the manufacturer for additional information.
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Affected products
Hybrid Recon 4.0
UPC: 00859873006158
Model: version 4.0.x*
Hybrid Recon 5.0
Model: version 5.0.0 VERSION 5.0
Why this matters
Performance issue
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 UPC code
The UPC is the barcode number on the packaging.
Affected UPCs: 00859873006158
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: version 4.0.x*, version 5.0.0 VERSION 5.0
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?
Performance issue
What should consumers do?
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. Performance issue
When was this product recalled?
This product was recalled on November 14, 2024.
Is the Hermes Medical Solutions, Ab brand affected by this recall?
Yes, Hermes Medical Solutions, Ab products are affected by this recall. This recall involves Hybrid Recon 4.0 and 5.0 medical devices. They are being recalled because of a performance issue where aspect and CT series may not align correctly. This could lead to incorrect alignment during reconstruction of studies. This recall is intended for the healthcare industry.