FDAMay 23, 2025device

SIGNA Architect AIR

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning. As a result, acoustic levels can exceed 99dB, the limit established by International Electrotechnical Commission (IEC 60601-2-33) when using hearing protection with a Noise Reduction Rating (NRR) of 29dB, as currently required in the Operator Manual.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems

UPCs

00195278283481

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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