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.
Other Recalls by Baxter Healthcare Corporation
- Class II: Risk 12/22/2025
- Class II: Risk 11/28/2025
- Class II: Risk 10/28/2025
- Class II: Risk 09/17/2025
- Class II: Risk 08/29/2025
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.