SIGMA SPECTRUM Infusion System (V8 Platform) (2020-11-26)

Starting date:

November 26, 2020

Posting date:

December 11, 2020

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-74523

Last updated:
2020-12-10

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  Reason
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  Affected products

Affected Products

SIGMA SPECTRUM Infusion System (V8 Platform)

Reason

Baxter Corporation is issuing an urgent medical device correction to the user level for the Spectrum Infusion Pumps due to a software error which may occur following the completion of a secondary infusion, during the programming of a repeat of that secondary infusion.

Affected products