B. Braun Perifix FX Contin Epidural Set Recall: Catheter Connector Leakage Risk

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Contact the company & request your remedy

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

B. Braun is recalling certain epidural sets that may leak or disconnect during use, which could lead to injury. This recall affects specific batch numbers of the Perifix FX Contin epidural set.

Why it’s dangerous

The catheter connectors in these sets may not stay securely closed during use. This can cause leakage or disconnection of the catheter from the connector, potentially leading to injury if anesthetic fluids leak or are administered incorrectly.

Who’s affected

Physicians using the CE17TF Perifix FX Contin epidural set with Material Number 332234 are affected. Those who have the specific batch numbers listed are at risk of injury from potential leakage or disconnection.

How to tell if you have this one

Check for the model CE17TF Perifix FX Contin epidural set with Material Number 332234. Affected units include batch numbers 61589584, 61617132, and 61622878.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Immediately
Discontinue use of the affected epidural set to prevent potential leakage or disconnection.

✎ GovInfoNow

Questions people ask

What batch numbers are affected?

Batch numbers 61589584, 61617132, and 61622878.

Why is this recall happening?

The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheter.

Is there a fix for this issue?

The recall record does not mention 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-3371-2018 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-3371-2018 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-3371-2018 (July 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3371-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 CE17TF PERIFIX FX CONTIN. EPIDURAL SET, Material Number 332234 Connection device used by physicians to provide various

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