ICU Medical 7" Ext Set w/MicroClave Recall: Incorrect Spin Collar Hazard

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Contact the company & request your remedy

Recalling firmICU Medical, Inc.951 Calle Amanecer · San Clemente, CA 92673-6212

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

ICU Medical is recalling 7" Ext Set w/MicroClave and Clave T-Connector sets due to an incorrect spin collar that could lead to improper connections during medical procedures. This recall affects specific lot numbers and model AH7262.

Why it’s dangerous

The incorrect spin collar may cause improper connections during medical procedures. This could lead to issues with fluid administration or device function. However, the hazard does not involve immediate risks like injury or death.

Who’s affected

Healthcare professionals using these medical devices are most at risk. Patients receiving treatments with the recalled sets could experience improper connections.

How to tell if you have this one

Check for the product name '7" Ext Set w/MicroClave' or 'Clave T-Connector' with model AH7262. Look for lot numbers 3483247, 3484722, or 3489328 on the label.

Brand
ICU Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the lot numbers 3483247, 3484722, or 3489328 on the device label.

✎ GovInfoNow

Questions people ask

What is the specific model number of the recalled product?

The model number is AH7262.

Which lot numbers are affected by this recall?

Lot numbers 3483247, 3484722, and 3489328 are affected.

Is there a fix or remedy for this issue?

The recall record does not specify a remedy.

Take action

Contact ICU Medical

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

✉️ Open in email

Subject: Recall Z-1344-2018 — ICU Medical ICU Medical

Hello,

I own a ICU Medical that is covered by recall Z-1344-2018 from ICU Medical.

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-1344-2018 (February 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1344-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 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.

ICU Medical, Inc. recalls 7" Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item AH7262. The firm name on

Lower-risk recall