GE Healthcare, LLC recalls DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.
- Recall date
- October 4, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1199-2018
- FDA classification
- Class II
- Brand / firm
- GE Healthcare, LLC
- Sold / distributed
- US Distribution to states of: AZ, IL NC, NH and PA.
Why it was recalled
Non-Conforming devices were shipped from the service center without proper evaluation and therefore may be nonconforming.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.
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