FDA Device recall Z-1839-2024
Achieva 3.0T Model Number (REF): (1) 781345
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Achieva 3.0T Model Number (REF): (1) 781345 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-1839-2024 |
| 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
Achieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4) 781277; (5) 781177
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) 781345 N/A; (2) 781344 N/A; (3) 781278 (01)00884838004139(21); (4) 781277 N/A; (5) 781177 N/A Serial Numb…UDI-DI: (1) 781345 N/A; (2) 781344 N/A; (3) 781278 (01)00884838004139(21); (4) 781277 N/A; (5) 781177 N/A Serial Numbers: 24079 34231 34256 34289 34220 34308 34139 34200 34213 34255 34258 34276 34301 34306 34020 34052 34082 34113 34120 34123 34230 34234 34235 34239 34240 34247 34260 34264 34270 34272 34274 34285 34287 34288 34297 34298 34299 34309 34312 34056 34282 34023 34144 34228 24115 34001 34095 34138 34143 34165 34269 34293 34300 34305 34115 34225 34253 34038 34047 34077 34126 34135 34160 34206 34254 34268 34275 34118 34237 34271 34273 34291 34242 34261 34290 34033 34104 34281 34086 34106 34125 34159 34241 34263 34286 34294 34295 34311 34022 34043 34208 34109 34130 34203 34207 34304 34074 34028 34029 34030 34034 34065 34066 34071 34073 34085 34201 34011 38295 38074 38191 38247 38254 38276 38326 38346 38355 38363 38285 38043 38073 38087 38092 38098 38108 38124 38140 38152 38157 38158 38171 38181 38185 38189 38190 38194 38196 38206 38209 38210 38212 38215 38216 38227 38231 38233 |
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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-1839-2024%22
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