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FDA (Device enforcement)Recalled 2022-11-10class ii

GE Medical Systems, LLC: Vivid q ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Ceph

Hazard

Potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire.

Details from the source

Reason for recall: Potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire. Distribution: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VI, VT, WA, WI, WV and the countries of Afghanistan, Albania, Algeria, Angola, Argentina, Armenia, Australia, Austria, AZERBAIJAN, Bahamas, Bahrai Quantity: 2,609 units Lot/code info: Model Number (System ID): H45021WZ (VQ20056, VQ20718, VQ020015, VQ20399, VQ202400, VQ20127, VQ20529, VQ20505, VQ20502, VQ20533, VQ20741, VQ20683, VQ20653, VQ20700, VQ20580, VQ20477, VQ20498, VQ020516, VQ020216, VQ20507, VQ20772, VQ20686, VQ20043, VQ20508, VQ20566, VQ20620, VQ20525, VQ20483, VQ20601, VQ20706, VQ20591, VQ20122, VQ20668, VQ020275, VQ20713, VQ20198, VQ20863, VQ20052, VQ20597, VQ20619, VQ20614, VQ020676, VQ20154, VQ20584, VQ20599, VQ20204, VQ20429, VQ20284, VQ20045, VQ20568, VQ20562, VQ020662, VQ20524, VQ20730, VQ20628, VQ20287, VQ20266, VQ20569, VQ20110, VQ20116, VQ20109, VQ20560, VQ20671, VQ20278, VQR20075, VQ20504, VQ20607, VQ20007, VQ20054, VQ20611, VQR020000, VQ20910, VQ20133, VQ20108, VQ20415, VQ20469, VQ20367, VQ20341, VQ20051, 516663VIVIDQ, VQ20755, VQ30010LO, VQ20715, VQ020732, VQ020745, VQ20585, VQ20288, VQ20412, VI002091, VQ20712, VQ20702, VQ20464, VQ20417, VQ20638, VQ20722, VQ20747, VQ20593, VQ20456, VQ20326, VQ20181, VQ20773, VQ20522, VQ20081, VQ20521, VQR20082, VQ20673, VQ20519, VQ20018, VQ020749, VQ20571, VQ020577, VQ20654, VQ20735, VQ20074, VIQ622774CART, VQ20458, VQ20841, VQ20867, VQ20828, VQ003479, VQ20721, VQ20067, VQ20436, VQ20512, VQ20493, VQ20497, VQ20592, VQ20501, VQ20587, VQ020587, VQ20265, VQ20743, 0911365659, 0911365660, 0911365688, 0911367268, 0911363889, 0911365759, 0911369227, 0911363789, 0911363467, 0911367212, 0911367113, 0911367322, 0911365546, 0911365614, 0911365651, 0911365542, 0911365630, 030081US02, 030232US13, 784271US01, 39073

UPC codes

082438030076, 082438040151, 082438040139, 082438040142, 082438040160, 082438040179, 082438040185, 082438040189, 082438040190, 082438040195, 082438020051, 082438230080, 082438030086, 082438150066, 082438160249, 082438160250, 082438160238, 082438160314, 082438160326, 082438100214, 082438100224, 082438100250, 082438230068, 082438090185, 082438230088, 082438120421, 082438120438, 082438120410, 082438120420, 082438120437, 082438160280, 082438160248, 082438160273, 082438070146, 082438120372, 082438120434, 082438080033, 082438150059, 082438150089, 082438120394

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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