PlainRecalls
FDA Devices Moderate Class II Terminated

DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.

Reported: April 4, 2018 Initiated: October 4, 2017 #Z-1199-2018

Product Description

DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.

Reason for Recall

Non-Conforming devices were shipped from the service center without proper evaluation and therefore may be nonconforming.

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
2
Distribution
US Distribution to states of: AZ, IL NC, NH and PA.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.. Recalled by GE Healthcare, LLC. Units affected: 2.
Why was this product recalled?
Non-Conforming devices were shipped from the service center without proper evaluation and therefore may be nonconforming.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 4, 2018. Severity: Moderate. Recall number: Z-1199-2018.