Baxter Healthcare Corporation: Device Recall

Recall #Z-0203-2026 · 08/29/2025

Class II: Risk

Recall Details

Recall Number
Z-0203-2026
Classification
Class II
Product Type
Device
Recalling Firm
Baxter Healthcare Corporation
Status
Ongoing
Date Initiated
08/29/2025
Location
Deerfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
27072

Reason for Recall

IV sets may leak.

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

Distribution Pattern

US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.