Smartperfusion and 2D Perfusion recall in Canada: Inaccurate performance
In plain language
This recall involves Smartperfusion and 2D Perfusion medical devices sold in Canada. They are being recalled because of technical issues that may lead to inaccurate presentations of data. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Smartperfusion
Model: RELEASE 1.0
Lot: More than 10 numbers, contact manufacturer.
2D Perfusion
Model: 001008
Lot: More than 10 numbers, contact manufacturer.
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: 001008, RELEASE 1.0
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?
This recall involves Smartperfusion and 2D Perfusion medical devices sold in Canada. They are being recalled because of technical issues that may lead to inaccurate presentations of data. Healthcare professionals should contact the manufacturer for more information.
What should consumers do?
Contact the manufacturer if you require 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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on March 3, 2023.
Is the PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. brand affected by this recall?
Yes, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. products are affected by this recall. This recall involves Smartperfusion and 2D Perfusion medical devices sold in Canada. They are being recalled because of technical issues that may lead to inaccurate presentations of data. Healthcare professionals should contact the manufacturer for more information.