- Recalling firm
- GE Medical Systems Information Technologies Inc
- Reason for recall
- GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).
- Affected products (lot / model / serial)
- no UDI, Serial Number or Sales Order Number: KSA7013962, KSA5646256, KSA5646267, KSA5646268, KSA5646321, KSA5646328, KSA5646242, KSA5646251, KSA5646257, KSA5646284, KSA5646289, KSA5646295, KSA5646297, KSA5646306, KSA5646314, KSA6689326, KSA6689333, KSA6689378, KSA7162600, KSA7162603, KSA7162619, KSA7162631, KSA7769614, KSA6017390, KSA6569811, KSA6569814, KSA6569816, KSA6569853, KSA6569856, KSA6569866, KSA6569875, KSA6569879, KSA6569896, KSA7162612, KSA7162623, KSA7162662, KSA6409156, KSA6409176, KSA6409177, KSA6409181, KSA6420012, KSA6420057, KSA6420088, KSA6420106, KSA7013897, KSA5646292, KSA6409244, KSA7162605, KSA6808884, KSA7304364, KSA7304449, KSA7304452, KSA6590164, KSA7304435, KSA6954216, KSA6954221, KSA6626645, KSA6689380, KSA6808843, KSA6808843, KSA6808873, KSA6808874, KSA6808897, KSA6808897, KSA6623262, KSA6945167, KSA6017455, KSA7096908, KSA7096928, KSA7096932, KSA7096935, KSA7096940, KSA7096941, KSA7096946, KSA7096959, KSA7096971, KSA7096976, KSA7096985, KSA7096986, KSA7096994, KSA7550169, KSA7304426, KSA6017413, KSA6420074, KSA7442867, KSA7520473, KSA6945379, KSA7495811, KSA7495812, KSA7495828, KSA7495833, KSA6623187, KSA6623188, KSA6623208, KSA6623241, KSA6623249, KSA6623265, KSA6623273, KSA6623282, KSA6664042, KSA6017434, KSA6017505, KSA6664062, KSA6664066, KSA7162592, KSA5646252, KSA7304361, KSA7304418, KSA6689310, KSA6689342, KSA7391408, KSA7391483, KSA7442814, KSA7442876, KSA5646246, KSA6017327, KSA6017337, KSA6017411, KSA6017418, KSA6017452, KSA7574793, KSA6899017, KSA6899063, KSA7013916, KSA7013926, KSA7013985, KSA6945142, KSA6945304, KSA7509846, KSA7509848, KSA7520466, KSA7520486, KSA7716910, KSA7716914, KSA7744944, KSA6409155, KSA6420064, KSA6626658, KSA6808891, KSA6808910, KSA7162609, KSA7304373, KSA7304430, KSA7162584, KSA7239702, KSA7304389, KSA7304427, KSA7304450, KSA7550170, KSA7590261, KSA7590265, KSA7590268, KSA7391447, KSA6590189, KSA6626712, KSA5646253, KSA5646280, KSA7495807, KSA7495816, KSA7495829, KSA6017341, KSA6017348, KSA6017362, KSA6017380, KSA6017469, KSA6017481, KSA5646296, KSA5646275, KSA5646276, KSA5646299, KSA5646307, KSA5646322, KSA6945203, KSA7442837, KSA7442886, KSA6590183, KSA7120771, KSA6945201, KSA7590244, KSA7590250, KSA7590255, KSA7667331, KSA5646244, KSA5646285, KSA5646287, KSA5646293, KSA5646301, KSA5646302, KSA5646305, KSA5646320, KSA5646330, KSA6945295, KSA6017345, KSA6017349, KSA6017354, KSA6017427, KSA6017482, KSA6017493, KSA6017500, KSA6017507, KSA6808932, KSA6017359, KSA6477222, KSA7509839, KSA7509841, KSA6964881, KSA6964929, KSA6590131, KSA6590148, KSA6590150, KSA6590165, KSA6590167, KSA6590171, KSA6590180, KSA6590182, KSA6590193, KSA6590196, KSA6590217, KSA6590220, KSA7442861, KSA6899014, KSA7716916, KSA7716917, KSA7716935, KSA6419990, KSA6420003, KSA6017330, KSA7550164, KSA7574776, KSA7239690, KSA7239706, KSA7239713, KSA6536472, KSA6536494, KSA6536534, KSA7676886, KSA7744939, KSA7744956, KSA6409197, KSA6409202, KSA6409203, KSA6409211, KSA6409217, KSA6409230, KSA6409240, KSA6409253, KSA6536445, KSA6536537, KSA7162660, KSA6420022, KSA6808878, KSA7716911, KSA7716912, KSA7716915, KSA7716919, KSA7716921, KSA7716932, KSA6899010, KSA6899041, KSA6899042, KSA6899076, KSA7304363, KSA7304440, KSA7442799, KSA7442817, KSA7442818, KSA7442821, KSA7442827, KSA7442838, KSA7442858, KSA7442870, KSA7442881, KSA7442891, KSA7485738, KSA7485755, KSA7485758, KSA7485761, KSA7485763, KSA7495820, KSA7495824, KSA7495825, KSA6649175, KSA6649203, KSA5646271, KSA5646298, KSA5646325, KSA5646250, KSA7442779, KSA7442784, KSA7442819, KSA7442830, KSA7442850, KSA7442853, KSA7442863, KSA6623220, KSA6623274, KSA7391414, KSA7391430, KSA7391453, KSA7391491, KSA6945297, KSA6945372, KSA6409167, KSA6017315, KSA6017503, KSA6536511, KSA6569838, KSA7716922, KSA7716926, KSA7716931, KSA7716937, KSA7716909, KSA7716930, KSA6623221, KSA6866913, KSA6866940, KSA6866941, KSA6866948, KSA6866964, KSA5646283, KSA5646313, KSA6017351, KSA6017365, KSA6017376, KSA6017463, KSA7509834, KSA6017334, KSA6017343, KSA6017381, KSA601
- Units affected
- 1249 units
- Distribution pattern
- Worldwide distribution.
- Firm location
- Waukesha, WI, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2245-2026
- Recall initiated
- April 24, 2026
- FDA classification date
- May 28, 2026
- FDA report date
- June 3, 2026
- FDA event ID
- 98938
- Last updated on HTM Vibe
- July 23, 2026