Ge Medical Systems Information Technologies Inc: Computer, Diagnostic, Programmable
GE CASE v7.0 Cardiac Testing System Recall Summary GE Medical Systems is recalling the CASE v7.0 Cardiac Testing System (Model 3031234-001) worldwide because the printer's electrostatic discharge brush can become dislodged, causing electrical sparking at the printer head that may ignite thermal paper and cause burns. The system has been distributed across the United States, Canada, and numerous countries in Europe, Asia, Africa, and the Middle East. This is a Class II recall affecting diagnostic cardiac testing equipment used in medical facilities.
- Recalling firm
- GE Medical Systems Information Technologies Inc
- Product
- CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
- Reason
- 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-24
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide distribution - US Nationwide and the countries of Algeria, Australia, Bangladesh, Cambodia, Canada, Croatia, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Indonesia, Ireland, Italy, Japan, South Korea, Lebanon, Libya, Lithuania, Malaysia, Myanmar, Netherlands, New...
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a17f3cba-a459-4be5-a239-529e92e469eb