Baxter recalls CLEARLINK SYSTEM CONTINU-FLO Solution Sets with potential leakage. This recall addresses a risk of IV fluid leaks that could cause complications during medical treatments.
IV sets may leak.
Baxter is recalling certain IV solution sets that may leak. This could lead to complications during medical treatments if the leak occurs.
The IV sets may leak, which could cause fluid to escape from the tubing during medical treatment. This leakage might lead to complications such as improper medication delivery or infection risks.
Patients receiving IV treatments using the recalled CLEARLINK SYSTEM CONTINU-FLO Solution Sets are affected. Healthcare providers using these sets for medical procedures are at risk.
Check for the product code 2C8571 and lot numbers R25B24055 on the packaging. The sets include a 104-inch (2.6 meters) tube with a 0.2 micron filter.
Look for the product code 2C8571 and lot numbers R25B24055 on the packaging.
The IV sets may leak, which could cause complications during medical treatments.
Check for the product code 2C8571 and lot numbers R25B24055 on the packaging.
The recall does not specify a remedy, so contact Baxter Healthcare Corporation for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0195-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0195-2026 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.
