Wireless Battery Module (2021-01-12)

Starting date:

January 12, 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-74873

Last updated:
2021-01-29

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  Reason
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  Affected products

Affected Products 

Wireless Battery Module

Reason

Baxter Corporation is issuing an urgent medical device correction to the user level for all Spectrum battery modules, due to customer reports of battery performance issues related to prolonged storage without recharging the battery. The affected battery modules are used with all versions of Spectrum infusion pumps.

Affected products