GE Healthcare MRI Systems recall: Software Issue

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model Number, Serial Number (System ID) : 2226300, 000000000R4938 (256329MR2); 2226300, 000000000R5598 (256ALOPMR); N/A, N/A (334699MR); 2377062-2, 00000002547YR8 (256265HMR); 5107849, 00000274691MR5 (205487MR2); 46-294231G1, 0002005-0411-5 (870972E16); 46-294231G1, 002005-1201-35 (623583MR1); 2377062-2, 00000963660YM6 (480323MR1); 5107849-2, 00000278561MR6 (818445MR); 46-294231G1, 002004-1028-04 (3825); 2377062, 00000941225YM5 (626335MR); 46-294231G1, 002004-0913-01 (3591); 46-294231G1, 002005-1018-15 (352333MR3T); N/A, N/A (954587MR1); 46-294231G1, 002002-0605-11 (781340MR); 5107849, 266201MR3 (RADNETMR1585); 46-294231G1, 002005-0110-28 (313593MR02); 5308573, 00000292781MR2 (609890MR); 2214149-2, 00000010224GQ4 (732745MR); 2377062-2, 00000963098YM9 (607798MREXCT); N/A, N/A (516825MR); N/A, N/A (405307NMR); N/A, N/A (814535MR1); 5107849-2, 00000283624MR5 (615588MRI); N/A, N/A (615473MR1); N/A, N/A (817922MRLX); 5107849-2, 00000278623MR4 (972378NSC3TMR1); 46-294231G1, 0002005-0823-7 (DZ1057MR01); 46-294231G1, 002006-0127-10 (DZ1193MR01); 2226300, 00000000R5456A (2722SIGNA15); 2226300, 000000000R6230 (4291EXC15T); 2226300, 000000000R4601 (MRR4601); 2226300, 000000000R4973 (0910272001); 2226300, 000000000R5899 (0910274027); M3000PT, 00000280570MR3 (0910273001); 46-294231G1, 002005-0511-13 (AZ1003MR01); 46-294231G1, 0000099-0111-2 (110037MR01); 46-294231G1, 002005-0301-06 (2560124); 2226300, 000000000R5054 (BA4073MR01); N/A, 000000000R6295 (2712857); 5308573, 00000290734MR3 (2771768); 2226300, 000000000R6853 (2776713); 5107849-2, 00000284596MR4 (1236631); 2226300, 000000000R5190 (1191369); N/A, N/A (270004); 2189500-3, 00000201911MR5 (22946-1); 46-294231G1, 002005-0301-18 (CATMR01); 46-294231G1, 000005-1212-11 (CRMR01); 2226300, 000000000R5504 (082427310017); 2215261, 00000215559MR6 (082427040057); 2226300, 000000000R5271 (082427040072); N/A, 00000243366MR2 (082427040040); 46-294231G1, 0000003-0315-2 (082427040061); 2226300, 000000000R6344 (082427040074); 5107849-2, 00000289798MR1 (082427100093); 5107849-2, 00000283174MR1 (082427140047); 5107849-2, 00000282831MR7 (082427140046); 5107849-2, 00000283662MR5 (082427210041); 5107849-2, 00000282959MR6 (2697548EXCITE); 2226300, 000000000R5692 (2694100HD); N/A, N/A (CY1028MR01); 2226300, 000000000R4124 (PC0114MR03); 46-294231G1, 000006-0425-19 (HC4719MR02); 5107849, 00000272346MR8 (CC5340MR02); N/A, 0002005-1020-4 (126597MR01); 46-294231G1, 0002005-0511-6 (125390MR01); 46-294231G1, 000091-0919-12 (PSTU02MR01); 2226300, 000000000R5851 (2704833SIGNA); N/A, 000000000R5205 (GF1002MR01); 2226300, 000000000R4942 (24527633818MRI); 46-294231G1, 002005-0519-10 (0828270022IB01); 46-294231G1, 002005-0216-12 (0828270021IB01); N/A, 0000006-0323-2 (HU1099MR01); 5107849-2, 00000284297MR9 (083027062101067); 5107849, 00000267657MR5 (083027826593614); 46-294231G1, 000007-0530-11 (083027592002490); N/A, N/A (083027062101391); 2226300, 000000000R5902 (083027602101557); N/A, N/A (0835270007); 2108800-2, 535779 (B5174306); 46-294231G1, 0002005-0714-6 (A126322002); N/A, N/A (B5183714); 2226300, 000000000R5542 (B5367312); 2377062-2, 00000963588YM9 (A6118004); N/A, N/A (A148761302); N/A, 00000189273MR6 (A5155133); 2226300, 000000000R5739 (A377686701); 2226300, 000000000R5390 (A6134706); 46-294231G1, 002001-0702-56 (A5104397); 2357500-3, 00000300710MR1 (A5739706); 46-294231G1, 002005-0805-20 (YM1503); 2226300, 000000000R4952 (YM1516); 2198999-2, 00000158807MR8 (YM0451); N/A, 000000000R4216 (JO1029MR01); 2226300, 000000000R1382 (0850270404); N/A, 00000271322MR0 (0850270094); 5107849, 00000282503MR2 (LV4038MR01); 46-294231G1, 0002005-1130-3 (1084MREINP); 5107849, 00000263976MR3 (MR262474MR0); 2377062-2, 00000963560YM8 (5606SIGNA); 46-294231G1, 002005-0411-13 (56MRE3TH2565370); 2226300, 000000000R5911 (813EXCITEHD); 2226300, 000000000R5037 (2640781MR-1); 2226300, 000000000R5966 (99251SIGNAHD); 46-294231G1, 000006-0403-14 (99201MR15); 2395001-2, 00000280669MR3 (0920279025); 46-294231G1, 0000099-0722-5 (0920279011); N/A, N/A (25565916MR); 2226300, 00000000R4926A (PL1530MR02); 46-294231G1, 000006-0308-13 (787740MOBILE); 5107849, 00000276591MR5 (787653MR3T); 46-294231G1, 0000006-0315-5 (787840CIRT3T); 46-294231G1, 002001-0530-30 (787840EXCITE); N/A, 000000000R5552 (RO1115MR01); 2226300, 000000000R5057 (RU1195MR01); 46-294231G1, 002005-1212-26 (600130MR02); 5107849, 00000275845MR6 (RU1283MR01); 46-294231G1, 000006-0412-16 (RU1296MR01); 2226300, 000000000R5862 (SA1014MR02); 2226300, 000000000R5545 (SA2051MR01); 2226300, 000000000R5699 (SA1041MR02); 46-294231G1, 002005-0328-20 (SA1004MR02); N/A, 002005-1018-11 (SA1006MR02); 2226300, 000000000R5764 (SA1021MR01); 2226300, 000000000R4655 (0847270017); 46-294231G1, 002005-1201-14 (ZA1180MR01); 2226300, 000000000R5102 (NPV31703); 2226300, 000000000R4415 (MPX33111); 2357500-2, 00000265818MR5 (MPX49302); 5107849, 00000275642MR7 (GEE34040); 2357500-2, 00000265818MR5 (MPX94700); 5107849, 00000278210MR0 (UPW21613); 2377062-2, 00000963343YM9 (DPI53205); 5107849, 00000267036MR2 (DPN62300); 46-294231G1, 0000094-0131-5 (DPM19607); 46-294231G1, 0000005-0209-1 (FPG33602); 5127452, 00000VALUE1177 (NPV77700); N/A, 002005-0627-13 (387040MR06); 2357500, 00000259106MR3 (0853270052IB1); N/A, N/A (0853270070); 46-294231G1, 0002005-0519-8 (0856270035); 2226300, 000000000R4976 (0856270037); N/A, N/A (0856270042); 5107849-2, 00000279892MR4 (06108MRS01); 46-294231G1, 002005-1201-26 (34006MRS03); 46-294231G1, 000006-0502-12 (35045MRS01); 2226300, 00000000R4866A (78004MRS01); N/A, N/A (45007MRS01); 5107849, 00000266746MR7 (54014MRS01); 2226300, 000000000R5885 63025MRS01); 2226300, 000000000R5892 (UK1015MR02); N/A, N/A (00133MRS02); N/A, N/A (05270MRS01); 46-294231G1, 002002-0221-13 (70065MRS02); 5107849-2, 00000280006MR8 (10079MRM73); 46-294231G1, 0000006-0511-7 (3882630908MRMET);

Product

GE Healthcare MRI Systems, Software Version 12.x, sold under the following product names: SIGNA MR/I ECHOSPD W/ EXCITE, 1.5 HISPEED HD 8-CH 400-AP, MR…

Recalling firm

GE Medical Systems, LLC

Quantity

5,200 total units

Distribution

Worldwide Distribution: US (nationwide) including states of:: AK, 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, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV; and countries of: Algeria, Argentina, Australia, Austria, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Bulgaria, Canada, Chile, CHINA, Colombia, Costa Rica, Croatia, CYPRUS, Czech Republic, DENMARK, Dominican Republic, Ecuador, Egypt, Estonia, Finland, France, Georgia, Greece, Guadeloupe, Guatemala, Guyana, Honduras, Hong Kong, Iceland, India, Indonesia, Iran, IRAQ, Ireland, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea (Republic of), Kuwait, Latvia, Lebanon, Libyan Arab Jamahiriya, Lithuania, Luxembourg, Macedonia, Malaysia, Mexico, Netherlands, New Zealand, Norway, Oman, Pakistan, Paraguay, Philippines, Portugal, Puerto Rico, Russia, Saudi Arabia, SINGAPORE, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Syria, Taiwan, Thailand, Turkey, United Arab Emirates, Uruguay, Uzbekistan, Venezuela, and Vietnam.

Recall date

October 24, 2018

Classification

Class II

Status

Terminated

Agency

FDA (device)