Baxter Healthcare recalls CLEARLINK SYSTEM EXTENSION SETs with potential leakage. This could cause IV fluids to leak, potentially leading to complications. Affected units have specific product codes and lot numbers.
IV sets may leak.
Baxter Healthcare is recalling certain CLEARLINK SYSTEM EXTENSION SETs because they may leak IV fluids. This could cause complications for patients receiving intravenous treatments. The recall affects specific product codes and lot numbers.
The extension sets may leak IV fluids during use. This could lead to complications such as fluid loss or contamination for patients receiving intravenous treatments. The hazard is not severe enough to cause serious injury in normal use.
Patients using intravenous treatments with the recalled extension sets are most at risk. Healthcare providers who use these sets for medical procedures may also be affected.
Check for product code 2C8634 and lot numbers R25A21024 on the extension set. The sets have a straight-type design with a 7.9-inch length and a retractable collar.
Look for product code 2C8634 and lot number R25A21024 on the extension set.
The extension sets may leak IV fluids, which could lead to complications for patients receiving intravenous treatments.
Check for product code 2C8634 and lot number R25A21024 on the extension set.
The recall record does not specify a remedy, so contact Baxter Healthcare directly for guidance.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0199-2026 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-0199-2026 from Baxter Healthcare. 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.