Baxter Healthcare Corporation: Medical Device Recall in 2023 - (Recall #: Z-1013-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Baxter Electrocardiograph, ELI 380 -DCS21

Product Classification:

Class II

Date Initiated: October 31, 2022

Date Posted: February 1, 2023

Recall Number: Z-1013-2023

Event ID: 91388

Reason for Recall:

One ELI 380 Electrocardiograph intended to be used for a pilot program was shipped to a customer by mistake on 26 October 2022.

Status: Terminated

Product Quantity: 1 unit

Code Information:

Lot number 122420001706

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated