GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-1198-2018)

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 TEC 7 ANESTHESIA VAPORIZER Is designed for the metered delivery of specific inhalation anesthetic agents for use in continuous flow techniques of inhalation anesthesia.

Product Classification:

Class II

Date Initiated: October 4, 2017

Date Posted: April 4, 2018

Recall Number: Z-1198-2018

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: 28

Code Information:

Model # M1107626 Mfg. Lot or Serial #: BEJN05568, BEJM03853, BEJM04539, BEJN05793, BEJP01947, BEJP03924, BEJP04380, BEJP08533, BEJU06631, BEJN06095, BEJP04706, BEJU05053, BEJM04542, BEJM04881, BEJM04901, BEJN07748, BEJN07849, BEJP03230, BEJP03239, BEJP03559, BEJP03984, BEJP05309, BEJP05347, BEJP05825, BEJP05834, BEJP05978, BEJP08567, and BEJP09304.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated