Baxter recalls Spectrum Wireless Battery Modules A/B/G/N (product code 36010) used with Spectrum V8 or IQ infusion pumps. These modules may fail to auto-document infusion status to hospital EMR systems, potentially causing data gaps in patient care.
The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.
Baxter is recalling Spectrum Wireless Battery Modules A/B/G/N (product code 36010) that may fail to automatically send infusion status information to hospital electronic medical records. This could lead to incomplete patient care documentation if the hospital's EMR system is integrated with the infusion pumps.
The battery modules may fail to send infusion status information back to the hospital's electronic medical record system. This software issue only affects facilities that have integrated the Spectrum V8 or Spectrum IQ infusion systems with their hospital EMR systems. The failure could result in incomplete patient care documentation.
Healthcare facilities using Spectrum V8 or Spectrum IQ infusion pumps with these battery modules are affected. Patients receiving infusion therapy through these systems may be at risk if their hospital's EMR system requires automatic documentation.
Check if your battery module has product code 36010. Look for serial numbers with radio software versions 22D28, 22D29, or 22D30. These modules are used with Spectrum V8 (35700BAX2) or Spectrum IQ (3570009) infusion pumps.
Verify your battery module's product code is 36010 and has serial numbers with radio software versions 22D28, 22D29, or 22D30.
No, the recall does not require immediate discontinuation. The hazard is specific to hospital EMR integration and does not cause immediate harm.
The recall does not apply if your hospital's EMR system is not integrated with the Spectrum V8 or Spectrum IQ infusion systems.
Check for product code 36010 and serial numbers with radio software versions 22D28, 22D29, or 22D30. These modules are used with Spectrum V8 (35700BAX2) or Spectrum IQ (3570009) infusion pumps.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2582-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-2582-2024 from Baxter Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
