Luminos dRF Max, MOBILETT Elara Max, YSIO Max and YSIO X.Pree
In plain language
This recall involves Luminos dRF Max, MOBILETT Elara Max, YSIO Max, and YSIO X.Pree medical devices sold in Canada. They are being recalled because magnetic connectors may affect implantable electronic devices like pacemakers. Maintain a safe distance from these devices if you have an implantable electronic device.
What to do
- Contact the manufacturer for additional information.
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Affected products
YSIO Max
Model: VE10ZA, VF10F_HF05, VF10K, VF10K_SP05, VF11H
Lot: 10762470
Luminos dRF Max
Model: VF10K_SP05
Lot: 10762471
MOBILETT Elara Max
Model: VF10K
Lot: 11107444
YSIO X.Pree
Model: VA10F_HF03
Lot: 11107464
Why this matters
May affect implantable electronic devices
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: 10762470, 10762471, 11107444, 11107464
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: VA10F_HF03, VE10ZA, VF10F_HF05, VF10K, VF10K_SP05, VF11H
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?
May affect implantable electronic devices
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?
Yes, there may be a health risk. May affect implantable electronic devices
When was this product recalled?
This product was recalled on July 5, 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 dRF Max, MOBILETT Elara Max, YSIO Max, and YSIO X.Pree medical devices sold in Canada. They are being recalled because magnetic connectors may affect implantable electronic devices like pacemakers. Maintain a safe distance from these devices if you have an implantable electronic device.