SIGNA Creator, SIGNA Explorer, NMRI systems
FDA Recall Z-1239-2025 · Posted 2025-02-28
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Recalling FirmGE Healthcare (China) Co., Ltd.
Recall StatusOpen, Classified
Product CodeLNH
Date Initiated2025-01-31
Product Quantity2538
Reason for Recall
For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.
Firm Action
On January 31, 2025, the firm notified customers through Urgent Medical Device Correction letters.
Customers were provided with instructions for continued use of their MR systems.
All potential users should be made aware of this safety notification and recommended actions.
If you have any questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative.
Root Cause
Software design
Distribution Pattern
Domestic US distribution nationwide. International distribution worldwide.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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