FDA Device recall Z-1851-2024
Ingenia Ambition X- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (R…
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Ingenia Ambition X- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (R… 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-1851-2024 |
| 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 X- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): (1) 782138; (2) 782109; (3) 781356
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) 782138 (01)00884838108622(21); (2) 782109 (01)00884838098350(21); (3) 781356 (01)00884838090040(21); Seri…UDI-DI: (1) 782138 (01)00884838108622(21); (2) 782109 (01)00884838098350(21); (3) 781356 (01)00884838090040(21); Serial Number 47194 47040 47092 47091 47048 47195 47345 47361 47050 47209 47246 47247 47293 47254 47275 47019 47049 47200 47356 47357 47197 47270 47013 47014 47015 47053 47065 47082 47099 47268 47274 47000 47002 47003 47017 47020 47024 47035 47047 47056 47058 47074 47078 47089 47097 47192 47225 47337 47226 47227 47341 47307 47364 47365 47372 47284 47350 47057 47075 47081 47088 47174 47175 47188 47193 47288 47052 47059 47072 47085 47184 47187 47211 47252 47262 47304 47328 47342 47384 47064 47244 47219 47220 47298 47094 47329 47096 47207 47283 47190 47264 47309 47034 47202 47315 47332 47367 47385 47016 47269 47382 47352 47012 47021 47221 47276 47297 47313 47314 47271 47281 47001 47032 47041 47248 47255 47258 47301 47311 47272 47306 47009 47023 47030 47080 47083 47189 47215 47222 47230 47231 47242 47245 47286 47299 47302 47310 47312 47004 47006 47007 47011 47018 47022 47025 4 |
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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-1851-2024%22
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