GE OEC Medical Systems, Inc OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 6800 digital mobile c arm is designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical, orthopedic, and extremity imaging. The device is not intended for whole body pediatric imaging. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 6800 digital mobile c arm is designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical, orthopedic, and extremity imaging. The device is not intended for whole body pediatric imaging.
Brand
GE OEC Medical Systems, Inc
Lot Codes / Batch Numbers
62-0212, 69-0054, 82-0023-RC, 82-0034, 82-0072, 82-0274, 82-0587, 8S-0668, 82-1710, 82-1803, 82-2147, 82-2620, 82-2754, 82-2815, 82-3014, 82-3234, 82-7010-MH, 86-0254, 86-0354, 86-1078, 89-0505, 89-0509, 89-0595, 89-0605, 89-0987, 89-1048, 89-1776, 89-1837, 89-2132, 89-2303, 89-2335, 89-2348, 89-2350, 89-2610, 89-2645, 8S-0066, 8S-0079, 8S-0341, 8S-0562, 8S-0615-C, 8S-0847, 8S-0849-C, 8S-1312, 8S-1971, 8S-2015-N, 8S-2116, 8S-2117, 8S-2199, 8S-2204, 8S-2320, 8S-2411, P4-0097-R, P4-0101-R, P4-0325-R, P4-0346-L, P4-0477-L, P6-0432-R, W2-0012, W2-0580-R, W2-0591-R, 82-0030
Products Sold
62-0212 , 69-0054 , 82-0023-RC , 82-0034 , 82-0072 , 82-0274 , 82-0587, 8S-0668 , 82-1710 , 82-1803 , 82-2147 , 82-2620 , 82-2754 , 82-2815 , 82-3014 , 82-3234 , 82-7010-MH , 86-0254 , 86-0354 , 86-1078 , 89-0505 , 89-0509 , 89-0595 , 89-0605 , 89-0987 , 89-1048 , 89-1776 , 89-1837 , 89-2132 , 89-2303 , 89-2335 , 89-2348 , 89-2350 , 89-2610 , 89-2645 , 8S-0066 , 8S-0079 , 8S-0341 , 8S-0562 , 8S-0615-C , 8S-0847 , 8S-0849-C , 8S-1312 , 8S-1971 , 8S-2015-N , 8S-2116 , 8S-2117 , 8S-2199 , 8S-2204 , 8S-2320 , 8S-2411 , P4-0097-R , P4-0101-R , P4-0325-R , P4-0346-L , P4-0477-L , P6-0432-R , W2-0012 , W2-0580-R , W2-0591-R , 82-0030
GE OEC Medical Systems, Inc is recalling OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 6800 digital mobile c arm is due to Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by th. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and
Recommended Action
Per FDA guidance
Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC sent an Urgent Safety Advisory Notices dated October 11, 2006 and February 21, 2007 via certified mail delivery letter to affected customers. The notices identified the affected products, problem and actions to be taken. Customers were informed that a GEHC OEC field service engineer would be contacting their facility to arrange to have a replacement hard disk drive installed on the affected system(s). Customers were instructed to ensure that images on the hard disk drive were stored via an alternate permanent media as the hard disk drive approaches the 170 image capacity until a GEHC OEC field service engineer had replaced the drive. For questions regardiug this issues contact the service team at 800-874-7378.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026