PRISMAX CONTROL UNIT (2021-10-05)

Starting date:

October 5, 2021

Posting date:

October 21, 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-76699

Last updated:
2021-10-22

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  Reason
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  Affected products

Affected Products

PRISMAX CONTROL UNIT

Reason

Baxter Corporation is issuing a correction for the Prismax. If the operator initiates therapy with a saved prescription and makes a change to the prescription after a disposable filter change using the same patient button, the Prismax may display values from the original prescription profile, rather than the current prescription.

Affected products