B. Braun Medical EPIDURAL TRAY 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

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

B. Braun is recalling an epidural tray used by doctors for anesthesia that may leak or disconnect catheters. This could lead to improper medication delivery or infection risks if the connection fails during use.

Why it’s dangerous

The catheter connectors may not stay closed during use, causing leakage or disconnection of catheters. This could lead to improper medication delivery or infection risks if the connection fails during anesthesia administration.

Who’s affected

Physicians using the CE17TOD epidural tray with batch numbers 61604903 or 61618120 are most at risk. Patients receiving anesthesia through this device could be affected if the connection fails.

How to tell if you have this one

Check for batch numbers 61604903 or 61618120 on the CE17TOD epidural tray. The product is a connection device used by physicians for anesthesia administration.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Leaks
Inspect the catheter connectors for signs of leakage or disconnection.
Stop Using if Leaks Observed
Immediately stop using the device if leakage or disconnection occurs.

✎ GovInfoNow

Questions people ask

What batch numbers are affected?

Batch numbers 61604903 and 61618120.

Is there a fix for this issue?

The recall does not provide a fix; users should check for leaks and stop using if problems occur.

How can I tell if I have the recalled product?

Look for the batch numbers 61604903 or 61618120 on the CE17TOD epidural tray.

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-3372-2018 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-3372-2018 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-3372-2018 (July 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3372-2018 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 CE17TOD CONT EPIDURAL TRAY LF, Material Number 332235 Connection device used by physicians to provide various

Use caution until it’s fixed