FDA Enforcement Class I Ongoing

Getinge Flow-e Anesthesia System, Part No. 6887900

Recall: Z-0961-2023 · Reported February 1, 2023

Enforcement

Recall Number
Z-0961-2023
Event ID
91339
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
Getinge Usa Sales Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 1, 2023
Initiation Date
December 22, 2022
Classification Date
January 26, 2023
Address
1 Geoffrey Way, N/A, Wayne, NJ, 07470-2035, United States

Description

Getinge Flow-e Anesthesia System, Part No. 6887900

Reason

Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. If gas delivery is stopped, a sustained decrease in delivered O2 concentration may lead to hypoventilation and hypoxia.

Code Info

Part # UDI 6887900 07325710010457 Serial Numbers 50012-50197 Software versions 4.8.0, 4.8.1, 4.8.2, and 4.8.3.

Distribution

US nationwide and Worldwide Distribution: Domestic distribution to AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA, WV. Foreign distribution worldwide.

Quantity

8.016 Total (7.766 OUS; 250 US)