XtremeCT
Brand(s)
Last updated
Summary
Product
XtremeCT
Issue
Medical devices - Performance
What to do
Identify device, quarantine device, take note of amendment/reinforcement of IFU.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| XtremeCT | 07110900 | SC3326 |
| XtremeCT | 06051201 | SC3319 |
Issue
The XtremeCT device is recalled due to potential safety risks. If the z-protection component detaches during a patient scan, it may cause injuries such as lacerations, skin abrasions, fractures, or hematomas to the arm or leg.
Recall start date: July 17, 2025
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies
Scanco Medical AG
Fabrikweg 2, Bruettisellen, Zurich, Switzerland, 8306
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77796
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