Health product recall

PrisMax Control Unit (2021-01-13)

Starting date:
January 13, 2021
Posting date:
January 29, 2021
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-74877

Last updated: 2021-01-29

Affected Products 

PrisMax Control Unit

Reason

Baxter Corporation is issuing an urgent medical device correction to the users of the Prismax control unit, due to the variability in performance of the tubing in the ARPS (automatic repositioning system) pump assembly which may lead to alarm situations during a system self-test and during therapy.

Affected products

PrisMax Control Unit

Lot or serial number

More than 10 numbers, contact manufacturer. 

Model or catalog number

955558

Companies
Manufacturer
Baxter Healthcare SA
PO BOX 8010
Zurich
8010
SWITZERLAND