ClearanceBrief
Recall Z-1401-2011 ยท LNH System, Nuclear Magnetic Resonance Imaging

Siemens Medical Solutions USA, Inc

MAGNETOM Verio Nuclear magnetic resonance imaging

DateFeb 23, 2011 (initiated Jan 10, 2011)
StatusTerminated
ReasonOn some systems the gradient cable connections did not meet firm's specifications after installation
Root causeOther
ActionSiemens Medical Solutions USA, Inc sent customers a letter on January 10, 2011 notifying them of an Update Instruction and informing them that recalling firm would preventatively check the gradient cable connections of all systems. For questions regarding this recall call 610-219-6300.
Quantity92
DistributionNationwide Distribution including AK, AZ, CA, CT, FL, HI, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NV, OH, OK, OR, PA, RI, TN, TX, VA, WI, and WV
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K072237MAGNETOM VERIO
Siemens Medical Solutions USA, Inc., Oct 10, 2007