FDA Device recall Z-1850-2024
Ingenia Ambition S Model Number (REF): (1) 782139
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Ingenia Ambition S Model Number (REF): (1) 782139 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-1850-2024 |
| 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 Ambition S Model Number (REF): (1) 782139; (2) 782133; (3) 782108; (4) 781359
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) 782139 (01)00884838108639(21); (2) 782133 N/A; (3) 782108 (01)00884838098343(21); (4) 781359 (01)008848380…UDI-DI: (1) 782139 (01)00884838108639(21); (2) 782133 N/A; (3) 782108 (01)00884838098343(21); (4) 781359 (01)00884838090057(21) Serial Numbers: Serial Number 48016 48053 48126 48003 48136 48285 48144 48020 48030 48124 48155 48191 48216 48218 48245 48300 48183 48186 48187 48222 48225 48234 48240 48241 48249 48269 48278 48284 48288 48293 48294 48299 48304 48313 48317 48326 48331 48051 48223 48207 48028 48031 48049 48050 48131 48134 48154 48160 48242 48254 48219 48000 48004 48005 48009 48019 48032 48132 48145 48224 48244 48040 48122 48039 48022 48152 48173 48012 48014 48036 48037 48044 48127 48151 48158 48174 48184 48043 48046 48047 48055 48128 48129 48153 48178 48180 48190 48192 48194 48226 48275 48181 48198 48199 48200 48023 48033 48045 48001 48038 48167 48185 48196 48236 48238 48239 48034 48276 48010 48170 48035 48172 48027 48248 48146 48147 48148 48163 48164 48165 48169 48182 48188 48271 48291 48297 48302 48303 48308 48309 48310 48329 48018 48283 48177 48011 48017 48056 48250 48272 |
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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-1850-2024%22
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