Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Baxter SIGMA Spectrum Infusion Pump V6 Recalled by Baxter Healthcare Corporation Due to Certain Spectrum infusion pumps may have an incorrect...

Date: June 20, 2025
Company: Baxter Healthcare Corporation
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.

Affected Products

Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX

Quantity: 14 units

Why Was This Recalled?

Certain Spectrum infusion pumps may have an incorrect version of software.

Where Was This Sold?

This product was distributed to 10 states: CA, FL, IL, KS, MI, MS, NY, OH, OK, VA

Affected (10 states)Not affected

About Baxter Healthcare Corporation

Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report