inforMED
MalfunctionLWP

ACCOLADE? EL DR

Received Jul 31, 2026 · Event occurred Jul 24, 2026

Report 2124215-2026-41154 · MDR key 50094413

Device

Generic name

Pacemaker

Model number

L321

Catalog number

L321

Lot number

724944

Product problems

  • Premature Discharge of Battery

Patient

Not reported

  • No Clinical Signs, Symptoms or Conditions

Narrative

Description of Event or Problem

It was reported that this pacemaker recorded a Code 1003, indicating the voltage is too low for the projected remaining capacity. A request was made to have data from this device analyzed. Data analysis identified potential high impedance within the battery. Continued monitoring was recommended. This device remains in service. No adverse patient effects were reported.

Additional Manufacturer Narrative

This product investigation is still in progress. This report will be updated when product investigation is complete.