B. Braun EPID 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 EPID trays that may leak or disconnect catheters during use. This could lead to improper anesthetic delivery or infection risks if the connection fails.

Why it’s dangerous

The catheter connectors may not stay closed, causing leakage or disconnection. This could lead to improper anesthetic delivery or infection risks if the connection fails during procedures.

Who’s affected

Physicians using the EPID tray for anesthetic delivery are most at risk. The recall affects specific batch numbers of the tray.

How to tell if you have this one

Check for batch numbers 61581429 or 61600731 on the EPID tray. The product is a medical device used by physicians for anesthetic 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 connector for signs of leakage or disconnection during use.
Stop Using if Leaking
Immediately stop using the tray if leakage or disconnection occurs.

✎ GovInfoNow

Questions people ask

What batch numbers are affected?

Batch numbers 61581429 and 61600731.

Is there a fix for this issue?

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

How can I tell if I have the recalled product?

The product is an EPID tray with batch numbers 61581429 or 61600731, used by physicians for anesthetic delivery.

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-3340-2018 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-3340-2018 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-3340-2018 (July 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3340-2018 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.

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