Official recall record
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-04-24
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00195278617644
- Brand on record
- GE Medical Systems Information Technologies Inc
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.
Record last checked against the registry on 2026-09-16.
Other recalls from this brand
- 2026-07-20 · US FDA — Medical Devices
PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353 - 2026-07-20 · US FDA — Medical Devices
PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592 - 2026-07-20 · US FDA — Medical Devices
PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209
All 12 official recall notices naming GE Medical Systems Information Technologies Inc on this site →
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