FDA Device recall Z-1849-2024
Ingenia 3.0T CX Model Number (REF): (1) 782105 (2) 781271
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Ingenia 3.0T CX Model Number (REF): (1) 782105 (2) 781271 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-1849-2024 |
| 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 3.0T CX Model Number (REF): (1) 782105 (2) 781271
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) (01)00884838098312(21); (2) (01)00884838068452(21) Serial Number 78121 78150 78157 78096 78208 78094 7801…UDI-DI: (1) (01)00884838098312(21); (2) (01)00884838068452(21) Serial Number 78121 78150 78157 78096 78208 78094 78012 78074 78154 78161 78170 78171 78172 78173 78182 78183 78189 78190 78196 78198 78205 78210 78212 78213 78216 78218 78221 78225 78233 78235 78238 78240 78241 78242 78243 78244 78250 78251 78252 78253 78256 78257 78262 78263 78265 78266 78267 78268 78269 78270 78271 78272 78273 78279 78280 78281 78282 78283 78284 78288 78289 78291 78292 78293 78294 78295 78296 78301 78305 78306 78307 78308 78309 78310 78312 78313 78314 78316 78317 78319 78320 78321 78322 78323 78327 78328 78329 78330 78332 78333 78334 78335 78338 78339 78340 78341 78342 78343 78345 78346 78347 78352 78353 78354 78356 78357 78358 78359 78360 78361 78362 78363 78364 78366 78368 78370 78374 78375 78376 78377 78386 78078 78080 78224 78098 78003 78017 78065 78070 78076 78081 78087 78097 78099 78101 78104 78107 78126 78149 78151 78181 78206 78219 78264 23032 78063 78064 78106 78187 78000 78005 78007 78009 780 |
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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-1849-2024%22
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