MAUDE manufacturer profile

ABBOTT · OJX

MAUDE profile for Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

Key facts

Manufacturer ABBOTT
Manufacturer group ABBOTT
Product code OJX
Product code name Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode

At a glance

  • 100–999 MAUDE reports
  • 1–9 Death reports
  • 100–999 Injury reports
  • 100–999 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • No Known Impact Or Consequence To Patient, No Clinical Signs, Symptoms or Conditions, Device Dislodged or Dislocated, Failure to Capture, High impedance, High Capture Threshold, Break, Capturing Problem Most reported problems

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About MAUDE manufacturer and product code profiles

Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

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