ClearanceBrief
Recall Z-2430-2010 ยท LNH System, Nuclear Magnetic Resonance Imaging

Philips Medical Systems North America Co. Phillips

Vista Nuclear Magnetic Resonance Imaging System, Picker International, Inc. World Headquarters 595 Miner Road Cleveland, Ohio 44143, U.S.A..

DateSep 17, 2010 (initiated Sep 19, 2008)
StatusTerminated
ReasonWater may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Root causeOther
ActionPhilips issued an Urgent Correction letter dated 09/19/2008 to their consignees, identifying the reason for the recall and the affected products. The firm issued the Field Change Order (FCO) 78100232. Field service engineers will visit each consignee and conduct an inspection of the magnets venting system of Edge, Vista, Eclipse, Polaris, Infinion, and Panorama 0.6T MRI systems. The consignees should contact the Philips Call Center at 1-800-772-9377, #5 #2 and reference "FCO 78100232".
Quantity16 units
DistributionNationwide Distribution: USA., including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WY. There is no distribution to foreign consignees.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K9315441.5T EDGE AND 1.0T VISTA SYSTEMS
Philips Medical Systems (Cleveland), Inc., Nov 22, 1993
K964626EDGE/VISTA SYSTEM ENHANCEMENT PACKAGE
Philips Medical Systems (Cleveland), Inc., Feb 10, 1997