Baxter Clearlink System Solution Set Recall: Inverted Clamps Cause Tubing Failure

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Contact the company & request your remedy

Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling specific lots of Clearlink System Solution Sets with Duo-Vent Spike because inverted side clamps can cause the tubing to become unusable. This could lead to treatment interruptions for patients using the medical device.

Why it’s dangerous

The recalled solution sets have side clamps that can invert, making the tubing unusable. This could interrupt medical treatments for patients. The issue is specific to certain lot numbers and does not cause immediate injury.

Who’s affected

Patients using the Baxter Clearlink System Solution Set with Duo-Vent Spike are affected. Healthcare providers who use the recalled lot numbers are most at risk of treatment interruptions.

How to tell if you have this one

Check for lot number DR24C15109 on the product packaging. The expiration date for this lot is March 16, 2026. The product is identified by reference number 2R8538.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot number DR24C15109 on the packaging or label.

✎ GovInfoNow

Questions people ask

What is the specific problem with these solution sets?

Inverted side clamps can cause the tubing to become unusable, potentially interrupting medical treatments.

Which lot numbers are affected?

Lot number DR24C15109 (expiring 3/16/2026).

Do I need to stop using this product?

No immediate action is required beyond checking the lot number. The remedy is not specified in the recall notice.

Take action

Contact Baxter

We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1010-2025 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1010-2025 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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Where this comes from

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.

Official source: FDA Recall #Z-1010-2025 (December 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1010-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Baxter Healthcare Corporation recalls Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538

Lower-risk recall