Health product recall

Wireless Battery Module

Last updated

Summary

Product
Wireless Battery Module
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Affected products

Affected products

Lot or serial number

Model or catalogue number

Wireless Battery Module

More than 10 numbers, contact manufacturer.

35223
36010

Issue

Baxter Corporation is issuing an urgent medical device correction for the Wireless Battery Modules (WBMs) used with Spectrum V8 and Spectrum IQ infusion pumps. Baxter is releasing a WBM software update that addresses a condition where Spectrum WBM may fail to autodocument infusion status information back to hospital's electronic medical record (EMR) system. This software issue only occurs when Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital's EMR system.

Recall start date: July 22, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Baxter Healthcare Corporation
1 Baxter Parkway, Deerfield, Illinois, United States, 60015
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-75890

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