Discovery™, Optima™ and SIGNA™ MR Systems
Brand(s)
Last updated
Summary
Product
Discovery™, Optima™ and SIGNA™ MR Systems
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Optima™ MR450w MRI System - Main Unit - 32ch | Not applicable. | M7004ZJ |
| SIGNA™ Premier | Not applicable. | SIGNA PREMIER |
| Discovery™ MR450 1.5t MR System - Main Unit | Not applicable. | DISCOVERY MR450 1.5T MR SYSTEM |
| Optima™ MR450w MRI System - Main Unit - Gem | Not applicable. | M7000YN |
| SIGNA™ PET/MR | Not applicable. | SIGNA PET/MR |
| SIGNA™ Architect | Not applicable. | SIGNA ARCHITECT |
| Discovery™ MR750 MR System - Main Unit | Not applicable. | DISCOVERY MR750 3.0T |
| Optima™ MR450w MRI System - Main Unit - 16ch | Not applicable. | OPTIMA MR450W 1.5T |
Issue
GE Healthcare has become aware that for certain MR systems the planned maintenance steps to check the functionality of the caster locks on the MR patient table may not have been performed.
Recall start date: June 30, 2025
Additional information
Details
Original published date:
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
Identification number
RA-77717
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