Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2131-2025 — SIGNA Architect AIR

U.S. FDA — Device Enforcement · United States · 2025-05-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2131-2025
Date of alert
2025-05-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Medical Systems, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00195278283481
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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