GE Medical Systems recalls Discovery MR750w 3.0T whole body MRI scanners due to potential loud acoustic noise during scans, which could cause discomfort or hearing damage. Affected units have specific system IDs listed in the recall notice.
Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
GE Medical Systems is recalling certain Discovery MR750w 3.0T MRI scanners because their gradient coils can produce loud noises during scans. This noise could cause discomfort or hearing damage for patients and staff if not properly managed.
The gradient coils in these MRI scanners can generate loud acoustic noise under specific scanning conditions. This noise may cause discomfort or hearing damage if not properly managed during scans.
Patients and medical staff using the recalled MRI scanners are most at risk. The recall affects specific models with unique system IDs listed in the official notice.
Check for the system IDs listed in the recall notice: 760724DVMR1, 214820TS750WMR, 281333MR2, 82427240081, 82427120136, 82427200092, or 82427250061. These IDs identify the affected scanners.
Identify your scanner's system ID by checking the label on the machine or contacting your facility.
The recall is for potential loud noise during scans, which could cause discomfort or hearing damage. The hazard is not immediately life-threatening but requires attention.
Check if your scanner has one of the specific system IDs listed in the recall notice: 760724DVMR1, 214820TS750WMR, 281333MR2, 82427240081, 82427120136, 82427200092, or 82427250061.
No, the recall does not require immediate stoppage. However, you should check the system ID and contact your facility for guidance on managing the noise.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0517-2025 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-0517-2025 from GE Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
