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.
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Contact the company
📍Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
✎ GovInfoNow plain-language explainer
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. Read more at govinfonow.com/recall/54604-baxter-spectrum-wireless-battery-modules-emr-documentation-failure-risk.
“Baxter Spectrum Wireless Battery Modules: EMR Documentation Failure Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54604-baxter-spectrum-wireless-battery-modules-emr-documentation-failure-risk. Based on FDA recall #Z-2582-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2582-2024%22&limit=1).
Baxter Healthcare Corporation voluntarily recalled Spectrum Wireless Battery Modules A/B/G/N, product code 36010, according to the FDA. The recall was announced on July 17, 2024, due to a software issue that may prevent the modules from auto-documenting infusion status information back to hospital Electronic Medical Record systems.
How to tell if you have it
Spectrum Wireless Battery Modules A/B/G/N
product code 36010
used with 35700BAX2 (Spectrum V8) and 3570009 (Spectrum IQ infusion pump)
Pump UDI/DI GTIN 00085412498683
Serial numbers with radio software versions 22D28, 22D29, and 22D30
UPC 00085412498683
The hazard
The Spectrum Wireless Battery Module may fail to auto-document infusion status information back to the hospital's Electronic Medical Record system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital's EMR system.
Context
GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since September 2, 2015. Other recent recalls by Baxter include a PRO+ MRS SURFACE FOR VERSACARE mattress recall on August 18, 2026, and recalls of 0.9% Sodium Chloride Injection and Dextrose 2000mL Bags on August 17, 2026. Other recent recalls of similar products include a Fresenius Kabi Ivenix Infusion System Software Recall on May 6, 2026, and an Elekta MOSAIQ Oncology System Software Recall on May 21, 2026.
How to tell if you have this one
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.
Brand
Baxter Healthcare
Product
Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US, Nationwide
Recall number
Product, codes & lots
Z-2581-2024
Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following: 35700BAX2 (Spectrum V8 infusion pump) or 3570009 (Spectrum IQ infusion pump) Baxter SIGMA Spectrum V8 Infusion Pump; Pump GTIN 00085412498683; All serial numbers with radio software versions 22D28, 22D29, and 22D30
Z-2582-2024
Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (Spectrum IQ infusion pump); Pump UDI/DI GTIN 00085412498683; All serial numbers with radio software versions 22D28, 22D29, and 22D30
Based on the official FDA remedy
What to do — step by step
Check Battery Module
Verify your battery module's product code is 36010 and has serial numbers with radio software versions 22D28, 22D29, or 22D30.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US, Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 42 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2582-2024 (July 17, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2582-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.