Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX
Reported: July 23, 2025 Initiated: June 20, 2025 #Z-2095-2025
Product Description
Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX
Reason for Recall
Certain Spectrum infusion pumps may have an incorrect version of software.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 14 units
- Distribution
- US States: CA, FL, IL, KS, MI, MS, NY, OH, OK, and VA.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX. Recalled by Baxter Healthcare Corporation. Units affected: 14 units.
Why was this product recalled? ▼
Certain Spectrum infusion pumps may have an incorrect version of software.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 23, 2025. Severity: Critical. Recall number: Z-2095-2025.
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