ClearanceBrief
Recall Z-3021-2017 ยท LNH System, Nuclear Magnetic Resonance Imaging

GE Medical Systems, LLC

Brivo 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, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images, spectroscopic images, parametric maps, and/or spectra, dynamic images of the structu

DateAug 2, 2017 (initiated May 11, 2017)
StatusTerminated
ReasonPossible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potential shock hazard.
Root causeMixed-up of materials/components
ActionConsignees received a written recall notice dated 05/17/2017 notifying them of a correction to all units using an Uninterruptable Power Supply. Consignees were instructed not to unplug the unit and to continue normal use. Units with the Eaton 9130 Uninterruptable Power Supply connected to the MR operator console would receive a correction at no charge. This would involve possibly replacing the power cable. GE Representatives will be contacting consignees to arrange corrections. Any questions can be directed to GE Healthcare Service at 1-800-437-1171 or your local service representative.
Quantity68 units in total
DistributionUS Nationwide in the states of : AK, CA, CO, CT, DE, FL, IA, IL, IN, KS, KY, LA, MD, MO, ND, NE, NJ, NY, OH, PA, TX, WA, and WI
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K103330BRIVO MR355, OPTIMA MR360
Ge Hangwei Medical Systems Co., Ltd., Feb 11, 2011
K120778BRIVO MR355
Ge Hangwei Medical Systems Co., Ltd., Mar 27, 2012
K123417BRIVO MR355, OPTIMA MR360
Ge Hangwei Medical Systems Co., Ltd., Jan 17, 2013