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Wireless Battery Module — recall 75890

Health Canada — Medical Devices · Canada · 2024-08-01 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
75890
Date of alert
2024-08-01
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/wireless-battery-module

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