Data Foundry

Medical device recalls 2024

CARESCAPE B650: Model Numbers: a) MBB313 — Class II medical device recall Z-2171-2024

Ongoing recall by GE Healthcare Finland Oy, reported 2024-07-03. GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Can

Recall numberZ-2171-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGE Healthcare Finland Oy, Helsinki, Finland
Recall initiated2024-04-05
Classified2024-06-21
Reported by FDA2024-07-03
Quantity54,800 units
UPC / GTIN / UDI-DI00840682143806, 00840682144308, 00840682146111
Serial numbers0089SA, 0180065HA, 022HA, 04SA, 0512073SA, 060HA, 090HA, 100, 1000, 1001, 1002, 10025HA, 1003, 1004, 1005, 1006, 1007, 1008, 1009, 101, 1010, 1011, 1012, 1013, 1014 and 475 more

Product

CARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416, 3) 2095801-001-01023150, 4) 2095801-001-01023151, 5) 2095801-001-01023152, 6) 2095801-001-01032962, 7) 2095801-001-01033915, 8) 2095801-001-01034302, 9) 2095801-001-01034399, 10) 2095801-001-01034528, 11) 2095801-001-01034573, 12) 2095801-001-01035087, 13) 2095801-001-01036384, 14) 2095801-001-01037712, 15) 2095801-001-01038022, 16) 2095801-001-01038593, 17) 2095801-001-01041035, 18) 2095801-001-01041611, 19) 2095801-001-01041694, 20) 2095801-001-01042512, 21) 2095801-001-01043771, 22) 2095801-001-01043810, 23) 2095801-001-01043815, 24) 2095801-001-01044650, 25) 2095801-001-01045256, 26) 2095801-001-01045394, 27) 2095801-001-01047045, 28) 2095801-001-01047175, 29) 2095801-001-01047424, 30) 2095801-001-01047840, 31) 2095801-001-01048362, 32) 2095801-001-01048417, 33) 2095801-001-01048980, 34) 2095801-001-01051456, 35) 2095801-001-01052158, 36) 2095801-001-01052233, 37) 2095801-001-01055544, 38) 2095801-001-01056326, 39) 2095801-001-01057436, 40) 2095801-001-01059243, 41) 2095801-001-01059748, 42) 2095801-001-01063874, 43) 2095801-001-01065225, 44) 2095801-001-01066765, 45) 2095801-001-01068762, 46) 2095801-001-01068763, 47) 2095801-001-01068789, 48) 2095801-001-01069489, 49) 2095801-001-01069499, 50) 2095801-001-01069511, 51) 2095801-001-01069736, 52) 2095801-001-01071206, 53) 2095801-001-01071246, 54) 2095801-001-01071369, 55) 2095801-001-01071456, 56) 2095801-001-01071457, 57) 2095801-001-01073465, 58) 2095801-001-01073479, 59) 2095801-001-01073480, 60) 2095801-001-01073804, 61) 2095801-001-01073821, 62) 2095801-001-01073831, 63) 2095801-001-01073833, 64) 2095801-001-01073842, 65) 2095801-001-01075357, 66) 2095801-001-01075506, 67) 2095801-001-01075588, 68) 2095801-001-01075714, 69) 2095801-001-01075924, 70) 2095801-001-01077403, 71) 2095801-001-01077441, 72) 2095801-001-01077461, 73) 2095801-001-01079833, 74) 2095801-001-01079863, 75) 2095801-001-01083142, 76) 2095801-001-01083734, 77) 2095801-001-01085418, 78) 2095801-001-01085443, 79) 2095801-001-01086276, 80) 2095801-001-01086712, 81) 2095801-001-01086761, 82) 2095801-001-01086774, 83) 2095801-001-01086812, 84) 2095801-001-01087472, 85) 2095801-001-01087477, 86) 2095801-001-01087541, 87) 2095801-001-01090666, 88) 2095801-001-01090675, 89) 2095801-001-01091331, 90) 2095801-001-01091461, 91) 2095801-001-01093653, 92) 2095801-001-01094099, 93) 2095801-001-01094103, 94) 2095801-001-01094107, 95) 2095801-001-01094246, 96) 2095801-001-01095946, 97) 2095801-001-01097590, 98) 2095801-001-01099368, 99) 2095801-001-01101966, 100) 2095801-001-01101967, 101) 2095801-001-01103899, 102) 2095801-001-01103993, 103) 2095801-001-01105509, 104) 2095801-001-01106417, 105) 2095801-001-01108128, 106) 2095801-001-01109198, 107) 2095801-001-01111183, 108) 2095801-001-01111184, 109) 2095801-001-01111601, 110) 2095801-001-01112917, 111) 2095801-001-01113476, 112) 2095801-001-01114061, 113) 2095801-001-01115803, 114) 2095801-001-01116299, 115) 2095801-001-01117382, 116) 2095801-001-01117424, 117) 2095801-001-01119791, 118) 2095801-001-01119805, 119) 2095801-001-01120649, 120) 2095801-001-01120762, 121) 2095801-001-01123351, 122) 2095801-001-01124300, 123) 2095801-001-01126694, 124) 2095801-001-01127783, 125) 2095801-001-01128064, 126) 2095801-001-01128764, 127) 2095801-001-01130112, 128) 2095801-001-01132721, 129) 2095801-001-01133150, 130) 2095801-001-01133492, 131) 2095801-001-01133517, 132) 2095801-001-01134200, 133) 2095801-001-01135675, 134) 2095801-001-01135943, 135) 2095801-001-01137569, 136) 2095801-001-01138299, 137) 2095801-001-01140050, 138) 2095801-001-01141178, 139) 2095801-001-01149187, 140) 2095801-001-01152254, 141) 2095801-001-01153436, 142) 2095801-001-01155553, 143) 2095801-001-01156974, 144) 2095801-001-01158167, 145) 2095801-001-011632

Reason for recall

GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650 monitors if, following the replacement of the CPU timekeeper battery, a mains power loss occurs during active monitoring. In the unlikely event that this occurs, it can result in the displays or monitors not turning on, after the mains power is restored. This can result in a delay in recognizing changes in patient condition until a replacement monitor is connected.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2171-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.