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
Other Recalls by Baxter Healthcare Corporation
- Class II: Risk 12/22/2025
- Class II: Risk 11/28/2025
- Class II: Risk 10/28/2025
- Class II: Risk 09/17/2025
- Class II: Risk 08/29/2025
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.