Luminos medical devices recall in Canada: potential injury risk
In plain language
This recall involves Luminos Lotus Max, dRF Max, and Agile Max medical devices sold in Canada. They are being recalled because a potential problem with the support arm could cause injury. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Luminos Lotus Max
Model: 11574100
Lot: 10230, 10185, 10287, 10207, 10203, 10074, 10235, 10237, 10045
Luminos dRF Max
Model: 10762471
Lot: 7865
Luminos Agile Max
Model: 10762472
Lot: 64198
Why this matters
Injury risk from support arm
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: 10230, 10185, 10287, 10207, 10203, 10074, 10235, 10237, 10045, 64198, 7865
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10762471, 10762472, 11574100
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?
Injury risk from support arm
What should consumers do?
Stop using the product immediately. Contact the manufacturer 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. Injury risk from support arm
When was this product recalled?
This product was recalled on August 19, 2024.
Is the Siemens Healthcare Gmbh brand affected by this recall?
Yes, Siemens Healthcare Gmbh products are affected by this recall. This recall involves Luminos Lotus Max, dRF Max, and Agile Max medical devices sold in Canada. They are being recalled because a potential problem with the support arm could cause injury. Stop using the product and follow the return/repair steps in the official notice.