أجهزة طبية
SIGNA™ Architect
تفاصيل الاستدعاء أدناه منشورة بالإنجليزية كما أصدرتها الحكومة الكندية دون تعديل. لم تنشر الحكومة صوراً لهذا المنتج.
Summary
| Type | Health product recall |
|---|---|
| Product | SIGNA™ Architect |
| Issue | Medical devices - Performance |
| What to do | Contact the manufacturer if you require additional information. |
| Audience | Healthcare |
| Brand(s) | Ge Medical Systems LLC |
| Last updated | 2026-10-16 |
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
SIGNA™ Architect |
PG75M2300263SC |
SIGNA ARCHITECT |
Issue
Incorrect liver stiffness measures from MR Touch protocol on certain MR systems
Details
| Original published date | 2026-10-16 |
|---|---|
| Alert / recall type | Health product recall |
| Category | Health products - Medical devices - Radiology |
| Companies | Ge Medical Systems LLC 3200 North Grandview Blvd, Waukesha, Wisconsin, United States, 53188 |
| Published by | Health Canada |
| Audience | Healthcare |
| Recall class | Type II |
| Recall date | 2026-10-09 |
| Identification number | RA-82807 |
Source: Government of Canada, Recalls and safety alerts – https://recalls-rappels.canada.ca/en/alert-recall/signatm-architect-0