FDA Device recall Z-1845-2024
Ingenia 1.5T Model Number (REF): (1) 782140
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Ingenia 1.5T Model Number (REF): (1) 782140 by Philips North America, citing the g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resultin….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1845-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-03 |
| Published | 2024-05-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Ingenia 1.5T Model Number (REF): (1) 782140; (2) 782115; (3) 782101; (4) 781396; (5) 781341; (6) 781315
Reason
The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
Identifiers
| code_info | UDI-DI: (1) 782140 (01)00884838108646(21); (2) 782115 (01)00884838099043(21); (3) 782101 (01)00884838098275(21); (4) 7…UDI-DI: (1) 782140 (01)00884838108646(21); (2) 782115 (01)00884838099043(21); (3) 782101 (01)00884838098275(21); (4) 781396 (01)00884838009820(21); (5) 781341 (01)00884838055322(21); (6) 781315 (01)00884838099715(21); Serial Numbers: 61019 61140 61080 61067 61091 61114 61028 61039 61040 61041 61000 61002 61003 61006 61009 61013 61017 61032 61058 61065 61066 61074 61075 61076 61097 61106 61124 61060 61001 61004 61008 61011 61023 61025 61026 61034 61035 61042 61046 61054 61055 61062 61063 61115 61078 61015 61119 61005 61020 61043 61085 61087 61088 61029 61030 61033 61036 61037 61045 61051 61052 61057 61061 61064 61068 61069 61070 61072 61095 61123 61116 61117 61125 61126 61129 61130 61027 61108 61109 61131 61144 61107 61138 61142 61143 61102 61103 61007 61014 61018 61016 61038 61073 61079 61024 61031 61059 61082 61084 61092 61093 61096 61101 61022 61044 61047 61049 61050 61053 61056 61094 61105 61112 61132 87260 70040 70229 70607 70763 84030 84108 84126 84234 84257 84596 87005 87146 7 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1845-2024%22
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