Health product recall

Luminos dRF Max, MOBILETT Elara Max, YSIO Max and YSIO X.Pree

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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