Zenition 70 and 50 recall in Canada: Performance issue
In plain language
This recall involves Zenition 70 and Zenition 50 medical devices sold in Canada. They are being recalled because a power issue can cause them to become unavailable for clinical use. Healthcare facilities should contact the manufacturer for more information.
What to do
- Contact the manufacturer, Philips Medical Systems Nederland B.V., for additional information.
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Affected products
Zenition 70
Model: 718133
Zenition 50
Model: 718096
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 model number
Model numbers are typically on the product label or packaging.
Affected models: 718096, 718133
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 Zenition 70 and Zenition 50 medical devices sold in Canada. They are being recalled because a power issue can cause them to become unavailable for clinical use. Healthcare facilities should contact the manufacturer for more information.
What should consumers do?
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?
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 October 10, 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 Zenition 70 and Zenition 50 medical devices sold in Canada. They are being recalled because a power issue can cause them to become unavailable for clinical use. Healthcare facilities should contact the manufacturer for more information.