---
title: "SIGNA Architect, Nuclear Magnetic Resonance Imaging System — FDA record Z-0518-2025 | Is It on Recall"
description: "Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning"
url: https://isitonrecall.com/recall/fda-device-z-0518-2025-signa-architect-nuclear-magnetic-resonance-imaging-system/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# SIGNA Architect, Nuclear Magnetic Resonance Imaging System — FDA record Z-0518-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 28, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: SIGNA Architect, Nuclear Magnetic Resonance Imaging System
- **Reason**: Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
- **Classification**: Class II
- **Recalling firm**: GE Medical Systems, LLC
- **Quantity**: 53 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0518-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0518-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI (01)00840682147095(11)240100(21)PG75M2400278SC, System ID 303467MR2; UDI/DI To be provided, System ID 1000005000; UDI/DI (01)00840682147095(11)220800(21)PG75M2300225SC, System ID 217528MR4; UDI/DI (01)00840682147095(11)220600(21)PG75M2200130SC, System ID 781SSHMR3; UDI/DI To be provided, System ID 301295AMR2; UDI/DI To be provided, System ID GON90303794; UDI/DI To be provided, System ID 215955HON3T; UDI/DI (01)00840682147095(11)230600(21)PG75M2300245SC, System ID 806UMCHWMR3T; UDI/DI (01)00840682147095(11)230800(21)PG75M2300255SC, System ID 703573ARC7; UDI/DI (01)00840682122702(11)220100(21)PG75A2300133SC, System ID 757953SPMR; UDI/DI (01)00840682147095(11)231000(21)PG75M2300263SC, System ID 905684MR3T; UDI/DI (01)00840682147095(11)220800(21)PG75M2200153SC, System ID 82427160355; UDI/DI To be provided, System ID 82427100482; UDI/DI To be provided, System ID 82427140330; UDI/DI To be provided, System ID 82427040333; UDI/DI To be provided, System ID 82427200209; UDI/DI To be provided, System ID 82427050061; UDI/DI To be provided, System ID 82427080138; UDI/DI (01)00840682147095(11)230400(21)PG75M2300232SC, System ID 82427150128; UDI/DI To be provided, System ID 82427200219; UDI/DI To be provided, System ID 82427080142; UDI/DI To be provided, System ID 82427230234; UDI/DI (01)00840682147095(11)231000(21)PG75M2300266SC, System ID 82427100499; UDI/DI To be provided, System ID 82427160405; UDI/DI To be provided, System ID 82427160407; UDI/DI (01)00840682147095(11)230600(21)PG75M2300247SC, System ID 82427160390; UDI/DI To be provided, System ID 82427160408; UDI/DI To be provided, System ID 82427160402; UDI/DI To be provided, System ID 82427120372; UDI/DI To be provided, System ID 82427120357; UDI/DI To be provided, System ID 82427120351; UDI/DI (01)00840682147095(11)230700(21)PG75M2300253SC, System ID 82427150130; UDI/DI (01)00840682147095(11)240100(21)PG75M2400276SC, System ID 82427030222; UDI/DI (01)00195278283481(11)231113(21)CNARC2300071TJ, System ID 82427030218; UDI/DI (01)00840682147095(11)230600(21)PG75M2300248SC, System ID 83027009451123; UDI/DI (01)00840682147095(11)240200(21)ANTAT2400005TJ, System ID MR00169; UDI/DI (01)00840682147095(11)240200(21)ANTAT2400004TJ, System ID MR00168; UDI/DI (01)00840682147095(11)240100(21)ANTAT2400001TJ, System ID MR00185; UDI/DI (01)00840682122702(11)180223(21)PG75A1800019MR, System ID 850270540; UDI/DI To be provided, System ID 850270791; UDI/DI To be provided, System ID LV4001MR03; UDI/DI (01)00840682147095(11)230600(21)PG75M2300246SC, System ID MRUA2408; UDI/DI To be provided, System ID P00434MR01; UDI/DI To be provided, System ID RF3138MR01; UDI/DI To be provided, System ID RU1838MR04; UDI/DI To be provided, System ID RF3580MR01; UDI/DI To be provided, System ID SA1058MR05; UDI/DI (01)00840682147095(11)221100(21)PG75M2200180SC, System ID FEG88320; UDI/DI (01)00840682147095(11)230800(21)PG75M2300256SC, System ID DE492A99; UDI/DI To be provided, System ID NEV439249; UDI/DI To be provided, System ID 853270212; UDI/DI To be provided, System ID 853270202; UDI/DI (01)00840682147095(11)230300(21)PG75M2300227SC, System ID 853270223 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide Distribution: US (nationwide) and OUS (foreign) to countries of: Canada, China, India, Japan, Korea, Latvia, Mexico, Poland, Russia, Saudi Arabia, Spain, and Taiwan.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Dec 4, 2024
- **Recall initiation date**: Oct 28, 2024
- **Center classification date**: Nov 22, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0518-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [GE Medical Systems, LLC records](https://isitonrecall.com/brand/ge-medical-systems-llc/)
