Baxter recalls certain CLEARLINK SYSTEM CONTINU-FLO Solution Sets due to potential leaks. This could cause IV fluids to leak from the tubing, potentially leading to complications during medical treatments.
IV sets may leak.
Baxter is recalling specific IV solution sets that may leak. This could cause IV fluids to leak from the tubing, potentially leading to complications during medical treatments.
The IV sets may leak due to a design issue with the tubing connections. Leaks could cause IV fluids to escape from the tubing, potentially leading to complications during medical treatments.
Healthcare professionals and patients using the recalled IV solution sets. Those with the specific product codes and lot numbers listed are most at risk.
Check for the product code 2C8537 and lot numbers R25A13055 through R25D19024 on the packaging or label. The sets include three CLEARLINK Luer Activated Valves, a backcheck valve, and a retractable collar.
Look for the product code 2C8537 and lot numbers R25A13055 through R25D19024 on the packaging or label.
The IV sets may leak due to a design issue with the tubing connections.
Check for the product code 2C8537 and lot numbers R25A13055 through R25D19024 on the packaging or label.
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-0193-2026 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0193-2026 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.
