Luminos Agile Max recall in Canada: collision risk
In plain language
This recall involves the Luminos Agile Max medical device sold in Canada. It's being recalled because a system malfunction could cause it to collide with the ceiling or wall. Contact the manufacturer for more information.
What to do
- Contact the manufacturer, Siemens Healthcare Gmbh, for additional information.
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Affected products
Luminos Agile Max
Model: 10762472
Lot: 61694
Why this matters
Collision risk
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: 61694
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10762472
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?
Collision risk
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. Collision risk
When was this product recalled?
This product was recalled on December 30, 2022.
Is the Siemens Healthcare Gmbh brand affected by this recall?
Yes, Siemens Healthcare Gmbh products are affected by this recall. This recall involves the Luminos Agile Max medical device sold in Canada. It's being recalled because a system malfunction could cause it to collide with the ceiling or wall. Contact the manufacturer for more information.