Description: 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 auto-document 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

Last Updated: Aug 1, 2024

Recall Number: RA-75890

CVE Number: N/A

Vendor Website: https://www.baxter.com – No recall information found

Additional Information: