Luminos dRF Max, MOBILETT Elara Max, YSIO Max and YSIO X.Pree
Brand(s)
Last updated
Summary
Product
Luminos dRF Max, MOBILETT Elara Max, YSIO Max and YSIO X.Pree
Issue
Medical devices - Device compatibility
What to do
Contact the manufacturer if you require additional information.
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| YSIO Max | VF10K_SP05 VF10K VF11H VE10ZA VF10F_HF05 | 10762470 |
| Luminos dRF Max | VF10K_SP05 | 10762471 |
| MOBILETT Elara Max | VF10K | 11107444 |
| YSIO X.Pree | VA10F_HF03 | 11107464 |
Issue
Siemens Healthineers was informed by the detector manufacturer that magnetic connectors may have been supplied as spare parts for portable detectors. If magnetic connection units are installed, a permanent (static) magnetic field is generated that exists independently of the operation of the detector. This can affect the function of implantable electronic devices such as pacemakers or implantable defibrillators if a minimum distance of >5 cm from the implanted device is not maintained.
Recall Start Date: June 18, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies
Siemens Healthcare Gmbh
Henkestr. 127, Erlangen, Germany, 91052
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-75792
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