Baxter Healthcare recalls Clearlink Non-DEHP Solution Set Luer Lock Adapter (Product Code 2R8401) due to potential leaks from the drip chamber. Affected units have specific lot numbers and expiration dates.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Clearlink Non-DEHP solution set listed below due to potential leaks originating from the drip chamber.
Baxter Healthcare is recalling a specific type of IV solution adapter because it may leak from the drip chamber. This leak could cause medication to spill, potentially leading to incorrect dosing or contamination.
The drip chamber in the adapter can leak, which might cause medication to spill. This could lead to incorrect dosing or contamination of the solution, especially in medical settings where precise measurements are critical.
Healthcare professionals using this adapter for intravenous therapy are most at risk. Patients receiving IV treatments with this specific model may be affected if leaks occur.
Check for the product code 2R8401 on the adapter. The lot number R23A02062 and expiration date of January 1, 2025 are also associated with this recall.
Identify the product code (2R8401), lot number (R23A02062), and expiration date (January 1, 2025) to confirm if your adapter is affected.
The recall is for potential leaks from the drip chamber, which could lead to medication spills or contamination. However, the hazard is not described as causing serious injury in normal use.
Check for the product code 2R8401, lot number R23A02062, and expiration date of January 1, 2025.
The recall does not specify a remedy, so you should check with Baxter Healthcare if you need further 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-1291-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1291-2024 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.
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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.
