B. Braun Filtered Triple-Leg Extension Set Recall: Potential occlusion risk

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Recalling firmB. Braun Medical, Inc.901 Marcon Blvd, N/A · Allentown, PA 18109-9512

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

B. Braun is recalling Filtered Triple-Leg Extension Sets (catalog number 477034) because they may become occluded or unable to prime. This could lead to treatment interruptions or complications during medical procedures.

Why it’s dangerous

The extension set may become blocked or unable to be primed, which could interrupt medication delivery or cause treatment complications during intravenous procedures.

Who’s affected

Healthcare professionals using the extension set for intravenous medication administration. Patients receiving treatments via this device are at risk if the set becomes occluded.

How to tell if you have this one

Check for the product catalog number 477034 on the packaging. Affected lots include 00SL713784, 0061741483, 0061755034, and 0061755296.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for the lot numbers 00SL713784, 0061741483, 0061755034, or 0061755296 on the packaging.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

B. Braun has identified potential for the extension set to become occluded or unable to prime based on complaints.

What should I do if I have this product?

Check the lot number on the packaging. If it matches the affected lots listed, contact B. Braun for further instructions.

Is there a fix for this issue?

The recall record does not specify a remedy or fix.

Take action

Contact B. Braun

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

✉️ Open in email

Subject: Recall Z-1509-2021 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-1509-2021 from B. Braun.

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-1509-2021 (March 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1509-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

B. Braun Medical, Inc. recalls Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage:

Lower-risk recall