FDA Device recall Z-2955-2018
GE Carestation 30 anesthesia systems
- FDA Device
- Class II
- terminated
- Published 2018-09-05
On 2018-09-05 the FDA classified a Class II recall of GE Carestation 30 anesthesia systems by Ge Medical Systems China, citing on systems equipped with the Auxiliary Common Gas Outlet (ACGO), there is a potential for the auxiliary gas switch to unexpectedly switch from the ACGO position back to the circle….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2955-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-24 |
| Published | 2018-09-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Medical Systems China |
| Distribution | n/a |
Product
GE Carestation 30 anesthesia systems
Reason
On systems equipped with the Auxiliary Common Gas Outlet (ACGO), there is a potential for the auxiliary gas switch to unexpectedly switch from the ACGO position back to the circle position. On systems equipped with the Aux O2 + Air function the switch could unexpectedly switch from the Aux O2 + Air position back to the circle position. These situations could lead to hypoxia.
Identifiers
| code_info | Serial Numbers: MF18045247 MF18045246 MF18055268 MF18055271 MF18055276 MF18055273 MF18055272 MF18055269 MF1805…Serial Numbers: MF18045247 MF18045246 MF18055268 MF18055271 MF18055276 MF18055273 MF18055272 MF18055269 MF18055274 MF18055270 MF18055275 MF18055277 MF18045265 MF18045233 MF18045181 MF18035153 MF18065338 MF18035144 MF18035151 MF18025067 MF18025066 MF18065336 MF18035142 MF18065335 MF18055299 MF18055300 MF18055302 MF18055298 MF18055301 MF18055303 MF18055304 MF18055305 MF18055306 MF18055307 MF18055308 MF18055309 MF18055310 MF18055311 MF18055312 MF18055313 MF18055314 MF18055315 MF18055316 MF18055317 MF18055318 MF18055319 MF18055320 MF18055321 MF18055322 MF18055323 MF18055324 MF18055325 MF18055326 MF18065345 MF18045266 MF18055267 MF18055285 MF18045227 MF18045228 MF18045225 MF18045229 MF18045230 MF18045248 MF18045249 MF18045250 MF18045251 MF18045252 MF18045253 MF18045254 MF18045183 MF18045184 MF18045182 MF18045185 MF18045186 MF18045187 MF18045188 MF18045189 MF18045190 MF18045191 MF18035158 MF18035163 MF18035164 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2955-2018%22
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