NA EXPRESS COIL - ANTERIOR ARRAYRecalls & reported problems
Ge Healthcare(Tianjin) Company Limited · 1.5T Anterior Array,Express Coil · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
6 other recalls cover devices cleared under the same FDA submission (K103330); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jan 31, 2025Open, Classified
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.
Z-1239-2025 · Root cause: Software design · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K103330. One submission often covers many models, so check the product and lot details in each record.
- Z-2478-2024 · Jun 14, 2024 · Open, ClassifiedOptima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
- Z-2477-2024 · Jun 14, 2024 · Open, ClassifiedBrivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
- Z-0610-2022 · Dec 23, 2021 · Open, ClassifiedGE Healthcare MR superconducting magnets, a component of GE Healthcare Brivo MR355/Optima MR360 System, nuclear magnetic resonance imaging system.
- Z-3021-2017 · May 11, 2017 · TerminatedBrivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, a
- Z-1209-2013 · Jun 8, 2012 · TerminatedGE Healthcare, Optima MR360/Brivo MR355 (HDsv), GE 0.35T Signa Ovation HD MR System, GE 0.2T Signa Profile HD MR System. Indicated for use as a diagnostic imaging device.
- Z-1433-2011 · Nov 9, 2010 · Terminated10) Brivo MR355/Optima MR360 Not yet 510(K) cleared and are not distributed in the US. (K103330) The Brivo MR355/ Optima MR360 is a whole body magnetic resonance scanner designed
Other System, nuclear magnetic resonance spectroscopic devices
- Ingenia Smartpath to dStream for 1.5TPhilips Medical Systems Nederland B.V. · System, nuclear magnetic resonance spectroscopic10 recalls131 reports
- Ingenia Ingenia 1.5TPhilips Medical Systems Nederland B.V. · System, nuclear magnetic resonance spectroscopic10 recalls24 reports
- Ingenia Ingenia 3.0TPhilips Medical Systems Nederland B.V. · System, nuclear magnetic resonance spectroscopic9 recalls9 reports
- Ingenia 1.5T CX 781262Philips Medical Systems Nederland B.V. · System, nuclear magnetic resonance spectroscopic8 recalls9 reports
- Achieva Achieva 1.5TPhilips Medical Systems Nederland B.V. · System, nuclear magnetic resonance spectroscopic3 recalls10 reports
- MAGNETOM Vida Fit 11410481Siemens Healthcare GmbH · System, nuclear magnetic resonance spectroscopic3 recalls1 report
- MAGNETOM Skyra Fit 11516217Siemens Healthcare GmbH · System, nuclear magnetic resonance spectroscopic2 recalls1 report
- MAGNETOM Cima.X 11689304Siemens Healthcare GmbH · System, nuclear magnetic resonance spectroscopic2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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