B. Braun Spinal/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 spinal/epidural trays that may leak or disconnect during use. This could lead to improper anesthetic delivery if the connector fails.

Why it’s dangerous

The catheter connectors may not stay closed during use, causing leakage or disconnection of catheters. This could lead to improper anesthetic delivery if the connector fails.

Who’s affected

Physicians using the GOVES1827K spinal/epidural tray with batch number 61608701 are affected. Those performing procedures requiring continuous anesthetic delivery are at highest risk.

How to tell if you have this one

Check for the model name 'GOVES1827K SPINAL/EPIDURAL TRAY (LF)' and batch number 61608701 on the device.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Leakage
Inspect the catheter connector for signs of leakage or disconnection.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates potential leakage or disconnection, so it is not safe to use without checking for issues.

What should I do if I have this product?

The recall does not specify a remedy, so contact B. Braun for further instructions.

How can I tell if I have the recalled product?

Look for the model name 'GOVES1827K SPINAL/EPIDURAL TRAY (LF)' and batch number 61608701.

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-3388-2018 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-3388-2018 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-3388-2018 (July 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3388-2018 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 GOVES1827K SPINAL/EPIDURAL TRAY (LF), Material Number 332614 Connection device used by physicians to provide various

Use caution until it’s fixed