FDA Enforcement Class II Ongoing

Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.

Recall: Z-2647-2023 · Reported October 4, 2023

Enforcement

Recall Number
Z-2647-2023
Event ID
92940
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Baxter Healthcare Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
October 4, 2023
Initiation Date
August 10, 2023
Classification Date
September 28, 2023
Address
1 Baxter Pkwy, N/A, Deerfield, IL, 60015-4625, United States

Description

Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.

Reason

Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical Device Correction for the Cardio Server E3 ECG Management System software listed below due to a report of the caliper tool becoming non-responsive, preventing the caliper function from being used temporarily on software versions v6.1.x, v6.2.x, and v7.0.x of the E3 user interface.

Code Info

a) v6.1.x, UDI/DI 00860991000355, all serial numbers, b) v6.2.x, UDI/DI 00860991000362, all serial numbers, c) v7.0.x, UDI/DI 00860991000379, all serial numbers

Distribution

Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AL, AR, AZ, CA, CA, CT, FL, FL, GA, IA, ID, IL, IN, KS, KY, MA, MD, MO, MS, MT, NE, NH, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA, WI, WV and the countries of Canada and Bermuda.

Quantity

89 units