Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-1009-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Baxter Solution Set with Duo-Vent Spike, REF 2R8404

Product Classification:

Class II

Date Initiated: December 20, 2024

Date Posted: January 29, 2025

Recall Number: Z-1009-2025

Event ID: 95929

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.

Status: Ongoing

Product Quantity:

Code Information:

UDI/DI 00085412676630, Lot Numbers: DR24C22079 (exp.3/247/2026), DR24H23086 (exp. 8/26/2026)

Distribution Pattern:

US Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.

Voluntary or Mandated:

Voluntary: Firm initiated