Health product recall

Prismaflex Control Unit (2019-10-11)

Starting date:
October 11, 2019
Posting date:
November 15, 2019
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-71601



Last updated: 2019-11-15

Affected Products

Prismaflex Control Unit

Reason

Baxter Corporation will be upgrading the software on Prismaflex control units to reduce the frequency of communication error alarms.

Affected products

Prismaflex Control Unit

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number
  • 107493
  • 113082
  • 114870
    Companies
    Manufacturer

    Gambro Lundia AB

    MAGISTRATSVAGEN 16, P.O. BOX 10101,

    Lund

    22010

    SWEDEN