Reported Sep 5, 2018 · Terminated

GE Carestation 30 anesthesia systems

GE Medical Systems China Co., Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Medical Systems China Co., Ltd. · National Hi-Tech · Wuxi, N/A · N/A

Is this the product you have?

  • GE Carestation 30 anesthesia systems
Lot codes and dates
  • Serial Numbers

    252 of 252 codes

    • 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
Amount recalled
252 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 16, 2020 · Data as of Sep 19, 6:14 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.