Baxter recalls non-vented CLEARLINK IV solution sets that may leak, risking infection. Affected units have specific product codes and lot numbers. Stop using immediately to prevent contamination.
IV sets may leak.
Baxter is recalling non-vented CLEARLINK IV solution sets that may leak, which could lead to infection if used improperly. This recall affects healthcare professionals and patients receiving IV treatments.
Leaking IV solution sets can introduce contaminants into the bloodstream, potentially causing infections. This hazard occurs when the non-vented design fails to maintain proper fluid pressure during use.
Healthcare providers and patients using IV treatments with the recalled CLEARLINK solution sets are most at risk. The recall applies to specific product codes and lot numbers.
Check for product code 2C8425 and lot numbers starting with R25C27086 on the packaging. The CLEARLINK SYSTEM Solution Set includes two Luer Activated Valves and is labeled as non-vented.
Discard the recalled IV solution set to prevent potential contamination.
The CLEARLINK SYSTEM Solution Set may leak, which could lead to infections if used improperly.
Product code 2C8425 with lot numbers starting with R25C27086.
Check for product code 2C8425 and lot numbers starting with R25C27086 on the packaging.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0191-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0191-2026 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.
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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.
