Baxter recalls non-vented CLEARLINK SYSTEM CONTINU-FLO Solution Sets with potential leakage. Leaks may cause infections during IV treatments. Affected units have specific product codes and lot numbers.
IV sets may leak.
Baxter is recalling certain CLEARLINK SYSTEM CONTINU-FLO IV solution sets that may leak. Leaks could lead to infections in patients receiving intravenous treatments. This recall affects specific product codes and lot numbers.
Leaking IV solution sets can introduce contaminants into the bloodstream, potentially causing infections. The non-vented design may allow fluid to escape if the set is not properly secured.
Healthcare providers using Baxter's CLEARLINK SYSTEM CONTINU-FLO Solution Sets for intravenous treatments are most at risk. Patients receiving IV therapy with these sets could face infection risks if leaks occur.
Check for product code 2R8519 and lot numbers starting with R25C26116. These sets have two CLEARLINK Luer Activated Valves and are labeled as 10 drops/mL, 9.6 feet long.
Verify your CLEARLINK SYSTEM CONTINU-FLO Solution Set has product code 2R8519 and lot numbers starting with R25C26116.
The recall is for potential leaks in the CLEARLINK SYSTEM CONTINU-FLO Solution Sets, which could lead to infections during IV treatments.
Look for product code 2R8519 and lot numbers starting with R25C26116 on the packaging.
The recall does not specify a remedy, so contact Baxter Healthcare Corporation for guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0201-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0201-2026 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.