Health product recall

Fresenius 2008T Hemodialysis System with CDX (2020-03-12)

Starting date:
March 12, 2020
Posting date:
April 17, 2020
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-72783



Last updated: 2020-04-17

Affected Products

Fresenius 2008T Hemodialysis System with CDX

Reason

There is a software issue and the "remove USB device 2" message error generated by the UI mics board is a symptom of that software anomaly.

Affected products

Fresenius 2008T Hemodialysis System with CDX

Lot or serial number

All lots.

Model or catalog number

190908

Companies
Manufacturer

Fresenius USA Inc.

4040 Nelson Avenue

Concord

94520

California

UNITED STATES