LUMINOS DRF MAX, UROSKOP OMNIA MAX, MULTITOM RAX
In plain language
This recall involves LUMINOS DRF MAX, UROSKOP OMNIA MAX, and MULTITOM RAX medical devices sold in Canada. They are being recalled because of a software defect that requires updated operator manuals. Contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
LUMINOS DRF MAX
Model: 10762471
Lot: More than 10 numbers, contact manufacturer.
UROSKOP OMNIA MAX
Model: 10762473
Lot: More than 10 numbers, contact manufacturer.
MULTITOM RAX
Model: 10860700
Lot: 11109, 11017, 11106, 11107, 11111, 11108
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: 11109, 11017, 11106, 11107, 11111, 11108, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10762471, 10762473, 10860700
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 LUMINOS DRF MAX, UROSKOP OMNIA MAX, and MULTITOM RAX medical devices sold in Canada. They are being recalled because of a software defect that requires updated operator manuals. Contact the manufacturer for more information.
What should consumers do?
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?
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 April 11, 2022.
Is the Siemens Healthcare Gmbh brand affected by this recall?
Yes, Siemens Healthcare Gmbh products are affected by this recall. This recall involves LUMINOS DRF MAX, UROSKOP OMNIA MAX, and MULTITOM RAX medical devices sold in Canada. They are being recalled because of a software defect that requires updated operator manuals. Contact the manufacturer for more information.