Baxter Healthcare Corporation: Device Recall

Recall #Z-2581-2024 · 07/17/2024

Class II: Risk

Recall Details

Recall Number
Z-2581-2024
Classification
Class II
Product Type
Device
Recalling Firm
Baxter Healthcare Corporation
Status
Ongoing
Date Initiated
07/17/2024
Location
Deerfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
17,377 units

Reason for Recall

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.

Product Description

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

Distribution Pattern

US, Nationwide

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.