inforMED
MalfunctionCGA

MEDLINE

Received Jun 19, 2026 · Event occurred May 21, 2026

Report 1417592-2026-02675 · MDR key 25563026

Device

Generic name

Meter,glucose,evencare G3,prof.use Only

Catalog number

MPH3540

Product problems

  • Device Provides Uninformative Message

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

IT WAS REPORTED THAT WHEN THE DEVICE IS TURNED ON IT SHOWS CODE 2029. THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS IS A REPORTABLE EVENT. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THIS REPORT WILL BE REOPENED AND REEVALUATED.

Description of Event or Problem

IT WAS REPORTED THAT WHEN THE DEVICE IS TURNED ON IT SHOWS CODE 2029.