Wireless Battery Module
Brand(s)
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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