AneurysmFlow (April 2026)
In plain language
This recall involves AneurysmFlow, a medical device used in aneurysm treatment. It's being recalled because the 'mafa ratio' it provides may not be reliable for clinical decisions, potentially leading to incorrect medical judgments. Healthcare professionals should contact the manufacturer for more information.
What to do
- Do not use the 'mafa ratio' from AneurysmFlow for clinical decision-making.
- Contact the manufacturer, Philips Medical Systems Nederland B.V., for additional information.
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Affected products
AneurysmFlow
Model: 1.4
Lot: Not applicable.
Why this matters
Unreliable medical information leading to incorrect clinical decisions
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: Not applicable.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 1.4
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?
Unreliable medical information leading to incorrect clinical decisions
What should consumers do?
Do not use the 'mafa ratio' from AneurysmFlow for clinical decision-making. Contact the manufacturer, Philips Medical Systems Nederland B.V., 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. Unreliable medical information leading to incorrect clinical decisions
When was this product recalled?
This product was recalled on April 2, 2026.
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 AneurysmFlow, a medical device used in aneurysm treatment. It's being recalled because the 'mafa ratio' it provides may not be reliable for clinical decisions, potentially leading to incorrect medical judgments. Healthcare professionals should contact the manufacturer for more information.