Reported Jun 10, 2026 · Ongoing

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

GE Medical Systems Information Technologies Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Medical Systems Information Technologies Inc · 9900 W Innovation Dr · Milwaukee, WI · 53226-4856

Is this the product you have?

  • CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Lot codes and dates
  • UDI-DI 00195278617644 Serial numbers

    1,835 of 1,835 codes

    • SU325232838SA
    • SU325032272SA
    • SU325293027SA
    • SU325222794SA
    • SU325122553SA
    • SU325363223SA
    • SU325483517SA
    • SU325152591SA
    • SU325363222SA
    • SU325483514SA
    • SU325272955SA
    • SU325222809SA
    • SU325092421SA
    • SU325272941SA
    • SU325272944SA
    • SU325393292SA
    • SU325393293SA
    • SU325393296SA
    • SU325443415SA
    • SU325303053SA
    • SU325353201SA
    • SU324512241SA
    • SU325032260SA
    • SU325433377SA
    • SU325242899SA
    • SU325242900SA
    • SU325192689SA
    • SU325172624SA
    • SU325172626SA
    • SU325172630SA
    • SU325333173SA
    • SU325383266SA
    • SU324502188SA
    • SU325112523SA
    • SU325112524SA
    • SU325192719SA
    • SU325313091SA
    • SU325403321SA
    • SU325323101SA
    • SU325323103SA
    • SU324502193SA
    • SU324502203SA
    • SU324502209SA
    • SU324502211SA
    • SU325272960SA
    • SU325272962SA
    • SU325252906SA
    • SU325433376SA
    • SU325473497SA
    • SU324502191SA
    • SU324502204SA
    • SU324502206SA
    • SU324502207SA
    • SU325293013SA
    • SU325293014SA
    • SU325293015SA
    • SU325293016SA
    • SU325383265SA
    • SU324482168SA
    • SU325122538SA
Amount recalled
1835

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 2:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.