Recall Z-0203-2026— Baxter Healthcare Corporation

Name: FDA recall Z-0203-2026
Creator: U.S. Food and Drug Administration
Published: 2025-08-29

Class II · Ongoing

Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2025-08-29. It names one FDA 510(k) clearance: K180739. Product: CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Activated Valve, 10 drops/mL, 107-inch (2.7 meters), Product Code 2R8858. Reason: IV sets may leak..

Recalling firm: Baxter Healthcare Corporation
Classification: Class II
Status: Ongoing
Initiated: 2025-08-29
Firm location: Deerfield, IL, United States

510(k) clearances named in this recall

1 on FDA's record

K180739 — Clearlink System Solution SetBaxter Healthcare Corporation·cleared 2019-05-28

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Activated Valve, 10 drops/mL, 107-inch (2.7 meters), Product Code 2R8858

Reason for recall

IV sets may leak.

Data sourced from openFDA. This site is unofficial and independent of the FDA.