GE Carestation 30 anesthesia systems — Class II medical device recall Z-2955-2018
Terminated recall by GE Medical Systems China Co., Ltd., reported 2018-09-05. On systems equipped with the Auxiliary Common Gas Outlet (ACGO), there is a potential for the auxiliary gas sw
| Recall number | Z-2955-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems China Co., Ltd., Wuxi, N/A, China |
| Recall initiated | 2018-07-24 |
| Classified | 2018-08-30 |
| Reported by FDA | 2018-09-05 |
| Terminated | 2020-12-16 |
| Quantity | 252 units |
| Serial numbers | MF18015046, MF18015047, MF18025059, MF18025060, MF18025061, MF18025062, MF18025063, MF18025064, MF18025065, MF18025066, MF18025067, MF18025068, MF18025069, MF18025070, MF18025071, MF18025072, MF18025073, MF18025074, MF18025075, MF18025076, MF18025077, MF18025078, MF18025079, MF18025080, MF18025081 and 227 more |
Product
GE Carestation 30 anesthesia systems
Reason for recall
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.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.