ProductGuru Recalls

Official recall record

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

Health Canada — Medical Devices · 2024-07-05 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-07-05
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: Health Canada — Medical Devices · Canada · all filters

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.