Discovery MR750w 3.0T, whole body magnetic resonance scanner
FDA Recall Z-0517-2025 · Posted 2024-11-22
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Recalling FirmGE Medical Systems, LLC
Recall StatusOpen, Classified
Product CodeLNH
Date Initiated2024-10-28
Product Quantity8 units
Reason for Recall
Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
Firm Action
GE Healthcare issued an "URGENT MEDICAL DEVICE CORRECTION" notice to its consignees on 10/28/20224 delivered through a traceable means. The notice explained the issue, safety issue, and requested the following actions be taken for the continued safe usage of the affected devices:
"Ensure hearing protection with a Noise Reduction Rating (NRR) of at least 33dB is used during exams on these systems. 200 pairs are provided with this letter.
Please post this letter in your facility on or near the MR operator console.
Please ensure all potential users in your facility are made aware of this safety notification and the recommended actions.
Please retain this document for your records."
Please complete and return the attached acknowledgement form to
[email protected].
For questions or concerns, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative.
Root Cause
Device Design
Distribution Pattern
Worldwide Distribution: US (nationwide) and OUS (foreign) to countries of: Canada, China, India, Japan, Korea, Latvia, Mexico, Poland, Russia, Saudi Arabia, Spain, and Taiwan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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