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Medical Device

CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3

Recall date: 2026-06-10 · Source: FDA_DEVICE
Brand / Firm
GE Medical Systems Information Technologies Inc
Product
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Reason for recall
Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of thermal printer paper. Ignition of the paper could potentially result in serious thermal injury.
Units affected
1835
Description
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
View official recall notice →