GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-1199-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: October 4, 2017

Date Posted: April 4, 2018

Recall Number: Z-1199-2018

Event ID: 79493

Reason for Recall:

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

Status: Terminated

Product Quantity: 2

Code Information:

Model 1100-9034-000 Mfg. Lot or Serial # BGBQ00675 and BGBQ01187

Distribution Pattern:

US Distribution to states of: AZ, IL NC, NH and PA.

Voluntary or Mandated:

Voluntary: Firm initiated