Artis Q, Icono and Pheno Systems recall in Canada: performance issue
In plain language
This recall involves Artis Q, Icono, and Pheno Systems medical devices sold in Canada. They are being recalled because a dedicated error detection mechanism may fail, preventing X-ray release. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer, Siemens Healthcare Gmbh, for additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Performance issue
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Performance issue
What should consumers do?
Contact the manufacturer, Siemens Healthcare Gmbh, 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 September 20, 2022.
Is the Siemens Healthcare Gmbh brand affected by this recall?
Yes, Siemens Healthcare Gmbh products are affected by this recall. This recall involves Artis Q, Icono, and Pheno Systems medical devices sold in Canada. They are being recalled because a dedicated error detection mechanism may fail, preventing X-ray release. Healthcare professionals should contact the manufacturer for more information.