GE 9100c NXT anesthesia systems — Class II medical device recall Z-2956-2018
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-2956-2018 |
|---|---|
| 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 | 401 units |
| Serial numbers | SPC18020055WA, SPC18020056WA, SPC18020057WA, SPC18020058WA, SPC18020059WA, SPC18020060WA, SPC18020061WA, SPC18020062WA, SPC18020063WA, SPC18020064WA, SPC18020065WA, SPC18020066WA, SPC18020068WA, SPC18020069WA, SPC18020070WA, SPC18020071WA, SPC18020072WA, SPC18020073WA, SPC18020074WA, SPC18020075WA, SPC18020076WA, SPC18020077WA, SPC18020078WA, SPC18020079WA, SPC18020080WA and 376 more |
Product
GE 9100c NXT 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
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2956-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.