FRED easyport (2019-04-13)

Starting date:

April 13, 2019

Posting date:

May 14, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type I

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69936

Last updated: 2019-05-14

• 
  Reason
• 
  Affected products

Affected Products

FRED easyport

Reason

In the course of an investigation triggered by two complaints regarding a malfunction during use, it was discovered that electrode material had been caught between a rivet and the ring terminal of the electrode cable leading to no or only intermittent electrical contact between the electrode and the defibrillator.

Affected products