inforMED
MalfunctionDTE

Dual Chamber Temporary Pacemaker

Received Jul 31, 2026 · Event occurred Jul 23, 2026

Report 2182208-2026-47217 · MDR key 50096347

Device

Generic name

Pulse-generator, Pacemaker, External

Manufacturer

Medtronic, Inc.

Model number

5392

Catalog number

5392

Product problems

  • Calibration Problem

Patient

Unknown

  • No Clinical Signs, Symptoms or Conditions