PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: April 4, 2018 Initiated: October 4, 2017 #Z-1198-2018

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.

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
28
Distribution
US Distribution to states of: AZ, IL NC, NH and PA.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
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.. Recalled by GE Healthcare, LLC. Units affected: 28.
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-1198-2018.