Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-2594-2025)

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:

Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519; intravascular administration set

Product Classification:

Class II

Date Initiated: August 8, 2025

Date Posted: October 1, 2025

Recall Number: Z-2594-2025

Event ID: 97447

Reason for Recall:

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.

Status: Ongoing

Product Quantity: 14400 units

Code Information:

UDI/DI 00085412048994, Lot Number R24I20079, Exp. 9/21/2026

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated