ProductGuru Recalls

Official recall record

Wireless Battery Module

Health Canada — Medical Devices · 2024-08-01 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-08-01
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

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

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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