Philips Hemodynamic Application recall in Canada: Performance issue
In plain language
This recall involves the Philips Hemodynamic Application software used in medical devices in Canada. It's being recalled because a performance issue may affect the accuracy of pressure wave data synchronization. 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
Philips Hemodynamic Application
Model: 002010
Lot: Not applicable.
Why this matters
Performance issue affecting data accuracy
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: 002010
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 affecting data accuracy
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?
Yes, there may be a health risk. Performance issue affecting data accuracy
When was this product recalled?
This product was recalled on May 16, 2024.
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 the Philips Hemodynamic Application software used in medical devices in Canada. It's being recalled because a performance issue may affect the accuracy of pressure wave data synchronization. Healthcare professionals should contact the manufacturer for more information.