Baxter Solution Set with Duo-Vent Spike: Inverted Clamps May Cause Tubing Unusable

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Contact the company & request your remedy

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling specific Solution Sets with Duo-Vent Spike that have a risk of inverted side clamps making the tubing unusable. This could disrupt medical treatment if the device is used without proper function.

Why it’s dangerous

Inverted side clamps in specific lots can cause the tubing to become unusable. This may lead to treatment interruptions if the device is not functioning properly. The issue is limited to specific model and lot numbers.

Who’s affected

Users of Baxter Solution Sets with Duo-Vent Spike (REF 2R8404) who purchased the affected lots (DR24C22079 and DR24H23086) are most at risk. Healthcare providers and patients using these devices may need to verify their product details.

How to tell if you have this one

Check for the product name 'Baxter Solution Set with Duo-Vent Spike' and lot numbers DR24C22079 (expires 3/24/2026) or DR24H23086 (expires 8/26/2026).

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify your lot number and expiration date to confirm if your device is affected.

✎ GovInfoNow

Questions people ask

What is the specific problem with these Solution Sets?

Inverted side clamps in specific lots can cause the tubing to become unusable.

Which lot numbers are affected?

Lot numbers DR24C22079 (expires 3/24/2026) and DR24H23086 (expires 8/26/2026).

Do I need to stop using this device immediately?

No immediate stop is required; check your lot number to see if it's affected.

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-1009-2025 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1009-2025 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-1009-2025 (December 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1009-2025 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 Solution Set with Duo-Vent Spike, REF 2R8404

Lower-risk recall