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:

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

FRED easyport

Lot or serial number

Not applicable.

Model or catalog number

0.900000
 

Companies
Manufacturer
Schiller AG
Altgasse 68
Baar
6341
SWITZERLAND