Baxter Solution Set with Duo-Vent Spike, REF 2R8404
FDA Recall #Z-1009-2025 — Class II — December 20, 2024
Product Description
Baxter Solution Set with Duo-Vent Spike, REF 2R8404
Reason for Recall
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
Recalling Firm
Baxter Healthcare Corporation — Deerfield, IL
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Distribution
US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.
Code Information
UDI/DI 00085412676630, Lot Numbers: DR24C22079 (exp.3/247/2026), DR24H23086 (exp. 8/26/2026)
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated